Oxidative Stress

46

Review clinical trials related to Oxidative Stress. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Oxidative Stress and Inflammatory Biomarkers in Gaucher Disease

The objective of this study is to evaluate oxidative stress and/or inflammation in patients with Gaucher disease type I using a series of biomarkers and correlate with measurements of currently used diagnostic biomarkers.

Participants needed: 34
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: University of MinnesotaUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

All participants must be 18 years or older. [+5]

Medically unstable conditions in any group as determined by the investigators [+5]

Status: Recruiting

Evaluation of the Effect of Hyperuricemia on Alveolar Bone Loss

Periodontitis is a multifactorial disease characterized by chronic inflammation of the gum tissue and alveolar bone destruction, and is known to be associated with various systemic diseases. Hyperuricemia, on the other hand, is a metabolic condition characterized by increased serum uric acid levels and can affect inflammation, oxidative stress, and bone metabolism. In recent years, the relationship between hyperuricemia and periodontal diseases has been increasingly investigated, but the biological mechanisms of this relationship have not yet been fully elucidated. Therefore, this study aimed to determine whether there is a relationship between hyperuricemia and periodontitis and to reveal the possible pathophysiological mechanisms of this relationship, which are shaped by inflammation, oxidative stress, and bone metabolism. A total of 80 individuals aged 18-65 years will be included in this clinical observational study. The periodontal status of the participants will be assessed using clinical periodontal parameters such as probing pocket depth, clinical attachment loss, plaque index, gingival index, and bleeding on probing. Participants will be divided into four groups according to their periodontal status and the presence of hyperuricemia: individuals with periodontitis and hyperuricemia, individuals with periodontally healthy and hyperuricemia, individuals with periodontitis but without hyperuricemia, and individuals with periodontally healthy and without hyperuricemia. Gingival crevicular fluid and serum samples will be taken from the participants. In these samples, receptor-mediated nuclear factor kappa B ligand, osteoprotegerin, total antioxidant status, total oxidant status, oxidative stress index, interleukin-1 beta, interleukin-10, interleukin-18, and nucleotide-binding oligomerization domain-like receptor protein 3 levels will be analyzed. This study is considered unique because it examines the relationship between hyperuricemia and periodontitis by evaluating inflammation, oxidative stress, and bone metabolism parameters together.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Recep Tayyip Erdogan University Training and Research HospitalUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Being between 18 and 65 years of age [+3]

Diabetes, cardiovascular disease, osteoporosis, chronic kidney disease, metaboli... [+5]

Status: Not yet recruiting

Effect of Cordyceps Supplementation Timing on Physiological Responses and Aerobic Adaptation in Athletes

Athletes frequently perform high-intensity exercise to improve physical performance and aerobic capacity. However, such training can induce exercise-induced muscle damage, oxidative stress, and inflammatory responses that may delay recovery and compromise subsequent training adaptations. Optimizing recovery strategies is therefore essential to maintain performance, reduce injury risk, and support long-term athletic development. Cordyceps is a medicinal mushroom that contains several bioactive compounds, including cordycepin and polysaccharides, which have demonstrated antioxidant, anti-inflammatory, and immunomodulatory properties. Although previous studies have reported beneficial effects of Cordyceps supplementation on exercise performance and physiological function, limited evidence exists regarding the optimal timing of supplementation relative to exercise. This study aims to investigate the effects of different Cordyceps supplementation timing strategies on physiological responses and aerobic adaptation following acute and chronic exercise training. Participants will be assigned to receive Cordyceps supplementation before exercise, after exercise, or placebo. The study will evaluate biomarkers of inflammation (IL-6), oxidative stress (MDA), muscle damage (CK), aerobic capacity (VO2max), and neuromuscular performance assessed using countermovement jump (CMJ) testing. The findings of this study are expected to provide evidence-based recommendations regarding nutritional recovery strategies and supplementation timing to optimize recovery and training adaptation in athletes and physically active individuals.

Participants needed: 30
Trial details
Age: 19-21Biological sex: MaleType: InterventionalSponsor: Surabaya State UniversityUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Male or female participants aged 19-21 years. [+5]

Current injury or musculoskeletal condition that limits participation in exercis... [+7]

Status: Recruiting

Acute Effects of Post-Exercise Hyperoxia on Recovery in Cycling

This study examines whether exposition to hyperbaric oxygen after a road-race simulation can help competitive cyclists recover and perform better the following day. Hyperbaric oxygen, which involves breathing oxygen inside a pressurized chamber, is used as a recovery method in elite and professional sport. Its effectiveness, however, remains controversial: despite this widespread use, there is a lack of solid scientific evidence that a single HBO session after strenuous endurance exercise actually improves recovery, or that clarifies how the amount of oxygen exposure influences any benefit. The study includes healthy male road cyclists between 18 and 40 years of age who compete at the national level in Belgium. After completing a fatiguing cycling session, each participant is randomly assigned to one of four groups receiving different levels of oxygen exposure during recovery. Two groups breathe oxygen under increased pressure inside a chamber at either 2.5 or 1.4 atmospheres absolute. A third group breathes oxygen at normal pressure. The fourth group receives a sham condition that reproduces the treatment setting without active oxygen exposure. The study is double-blind, meaning that neither the participants nor the researchers assessing the outcomes know which condition each participant receives. The main goal is to determine whether a single session of post-exercise HBO improves next-day endurance performance, and whether higher oxygen exposure produces greater effects. The researchers also collect blood samples and physiological measurements to better understand how the body recovers.

Participants needed: 48
Trial details
Age: 18-40Biological sex: MaleType: InterventionalSponsor: Université Catholique de LouvainUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Road cyclists competing in Elite 2 (Elite without professional contract) or Unde... [+4]

Presence of significant cardiovascular, pulmonary, neurological, ENT, or metabol... [+4]

Status: Not yet recruiting

Human Pilot Study for the Investigation of the Role of Bilberry and Olive Bioactives on Oxidative Stress Parameters and Inflammatory Markers.

Numerous plant-based foods contain bioactive compounds, in particular polyphenols, which have antioxidant, anti-inflammatory, and metabolic regulatory effects. These so-called food bioactives (FB) are converted in the human organism, in particular by the gut microbiota and microsomal (liver/intestinal) metabolism, into numerous metabolites, which often represent the actual biologically active molecules. As part of the European HORIZON-MSCA Doctoral Network "BioTransform," two such food models are being studied as examples: 1. Olive products (Olea europaea L.) - representative of the Mediterranean diet, rich in secoiridoids and phenylethanols (especially hydroxytyrosol and tyrosol). 2. Bilberry /blueberry (Vaccinium myrtillus L.) - representative of the Central European diet, rich in anthocyanosides. Two parallel human intervention studies will be conducted, one in Graz (WP1, DC5) and one in Athens (WP1, DC3). These pilot studies will generate biological samples (blood, urine, stool) and investigate the extent to which taking these standardized dietary supplements influences glucose metabolism and markers of oxidative stress and low-grade inflammation.

Participants needed: 60
Trial details
Age: 30-50Biological sex: AllType: InterventionalSponsor: National and Kapodistrian University of AthensUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

30-50 years old, [+6]

No signed informed consent [+5]

Status: Not yet recruiting

Polyphenol Intake, Mediterranean Diet Adherence, and Oxidative Stress in Pregnancy

This study is a randomized controlled clinical trial designed to evaluate the effect of a polyphenol-rich dietary intervention during pregnancy on endothelial function, oxidative stress biomarkers, and maternal and neonatal outcomes. Pregnancy is associated with metabolic and vascular adaptations, and complications such as gestational diabetes and hypertensive disorders are linked to endothelial dysfunction and increased oxidative stress. Dietary factors, particularly adherence to the Mediterranean diet and intake of polyphenol-rich foods, may play a protective role. Pregnant women will be randomly assigned to either an intervention group or a control group. The intervention consists of daily consumption of 10 g of natural non-alkalized cocoa and structured dietary counseling aimed at achieving at least five daily servings of fruits and vegetables, alongside general Mediterranean diet recommendations. The intervention will last 12 weeks, from early to mid-pregnancy. Biomarkers of endothelial function and oxidative stress will be measured at different time points, along with clinical maternal outcomes (including gestational diabetes and hypertensive disorders) and neonatal outcomes. The aim is to determine whether this dietary intervention improves endothelial function, reduces oxidative stress, and contributes to better pregnancy outcomes.

Participants needed: 60
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of SalamancaUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Pregnant women aged 18 years or older. [+5]

Medical or obstetric conditions that contraindicate dietary modifications. [+7]

Status: Not yet recruiting

Impact of Electronic Cigarette Temperature and Solvent on Biomarkers

This project seeks to determine how e-cigarette (EC) physical design features, including those that allow the user to manipulate the quality and quantity of aerosols, affect exposure and toxicity from oxidants and other aerosol constituents.

Participants needed: 50
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: Milton S. Hershey Medical CenterUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

21 years of age or older [+6]

Women who are pregnant and/or nursing or trying to become pregnant [+4]

Status: Recruiting

Little Cigar Oxidants

Determine the effects of little cigars on human exposure to tobacco smoke oxidants. In a balanced randomized cross-over study design in cigarette smokers, subjects will be assigned to 3 exposure groups. These include a high oxidant little cigar exposure condition, a low oxidant little cigar exposure condition, and their usual cigarette. Biological samples will be collected before and after product usage.

Participants needed: 50
Trial details
Age: 21-65Biological sex: AllType: InterventionalSponsor: Milton S. Hershey Medical CenterUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Aged 21 - 65 years old [+7]

Women who are pregnant and/or nursing or trying to become pregnant [+4]

Status: Not yet recruiting

Hyaluronic Acid as an Adjunct to Non-Surgical Periodontal Therapy in Smokers

The goal of this clinical trial is to evaluate whether hyaluronic acid (HA) improves periodontal healing in people with periodontal disease who smoke. Moreover, the effects of HA on biomolecules and bacteria levels will be assessed during the follow up period. The main questions it will answer are: Will periodontal sites treated with HA gel after non-surgical periodontal treatment (NSPT) lead to better outcomes in clinical parameters compared to the sites treated with NSPT only in smokers? Will adjunctive use of HA gel reduce oxidative stress markers and bacteria levels during follow-up? Researchers will compare periodontal sites receiving NSPT with adjunctive HA gel application to sites receiving NSPT alone to determine whether HA provides additional clinical, biochemical and microbiological benefits. Participants will: * first receive full-mouth NSPT then, randomization will be performed in selected jaw to determine the test sites. These two interproximal test sites will additionally receive HA gel application. * attend follow-up visits at 1, 3 and 6 months for clinical periodontal measurements and to provide gingival crevicular fluid samples (GCF) and subgingival samples. The GCF samples will be evaluated for Metallothionein (MT) and 8-hydroxy-2'-deoxyguanosine (8-OHdG) levels and subgingival samples for periodontal pathogens.

Participants needed: 23
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Marmara UniversityUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Individuals who sign the informed consent form [+5]

Individuals who do not sign the informed consent form [+4]

Status: Recruiting

Effects of Royal Jelly Supplementation in Chronic Kidney Disease

The objective of this study is to evaluate the effects of royal jelly on inflammation and cellular senescence in patients with chronic kidney disease (CKD) on hemodialysis (HD).

Participants needed: 30
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Universidade Federal FluminenseUpdated: May 18, 2026Locations: 1
Eligibility criteria

patients with CKD undergoing hemodialysis for more than 6 months [+1]

pregnant, [+5]

Status: Not yet recruiting

Ginger in the Modulation of Inflammatory Cytokines and Oxidative Stress in Patients With Coronary Artery Disease

The study aims to evaluate the effect of ginger supplementation on inflammatory cytokines and markers of oxidative stress in patients with Coronary Artery Disease (CAD). A longitudinal double-blind randomized clinical trial will be carried out, involving CAD participants for two months.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Universidade Federal FluminenseUpdated: May 19, 2026Locations: 1
Eligibility criteria

Both sexes [+5]

Unstable Coronary Artery Disease; [+5]

Status: Recruiting

Red Propolis Supplementation as a Strategy in Chronic Kidney Disease

The objective of this study is to evaluate the effects of red propolis on inflammation and oxidative stress in patients with chronic kidney disease on conservative management.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Universidade Federal FluminenseUpdated: May 19, 2026Locations: 1
Eligibility criteria

patients with CKD stages 3-5 under conservative management

pregnant, [+5]

Status: Not yet recruiting

Effects of Royal Jelly and Propolis on Metabolomic Signatures, Inflammation, and Cardiovascular Risk in Patients With Coronary Artery Disease.

The aim of this project is to evaluate the effect of bioactive compound sources, propolis and royal jelly, on metabolomics, inflammation, and cardiovascular risk markers in participants with coronary artery disease. A longitudinal double-blind randomized clinical trial will be carried out, involving CAD participants for two months.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Universidade Federal FluminenseUpdated: May 19, 2026Locations: 1
Eligibility criteria

Both sexes [+5]

Unstable Coronary Artery Disease; [+5]

Status: Recruiting

Cerebral Blood Flow and Ventilatory Responses During Sleep in Normoxia and Intermittent Hypoxia

A prospective double blind, placebo-controlled, randomized cross-over trial to evaluate the effect of lowering cerebral blood flow on the ventilatory chemoreflexes (acute hypoxic and hypercapnic ventilatory responses).

Participants needed: 12
Trial details
Phase: Phase 1, Phase 2Age: 18-45Biological sex: AllType: InterventionalSponsor: University of CalgaryUpdated: May 1, 2026Locations: 1
Eligibility criteria

Healthy adults [+4]

Cerebrovascular, cardio-respiratory, renal and metabolic diseases [+4]

Status: Not yet recruiting

Mediterranean Diet and Oxidative Stress in Type 1 Diabetes (MEDOX-T1D)

Achieving optimal glycemic control in type 1 diabetes requires a holistic approach that includes individualized medical nutrition therapy in addition to appropriate insulin therapy. When diabetes is poorly managed, metabolic control is impaired. Hyperglycemic events increase oxidative stress in the body and can lead to complications. The aim of this study is to examine the effect of a 12-week Mediterranean diet on oxidative stress markers in children with type 1 diabetes who do not meet the metabolic target (HbA1c \> 7%) and whose adherence to the Mediterranean diet is "poor" and "needs improvement". The study, planned between March 2026 and March 2027, will be conducted with girls aged 10-18 years with type 1 diabetes who are followed up at the Department of Pediatric Endocrinology, Istanbul Faculty of Medicine, Istanbul University. In the first phase, participants were divided into groups based on their HbA1c levels: those with HbA1c ≤ 7 met the metabolic target (Group A); Those with HbA1c \> 7 will be divided into two groups: those not meeting the metabolic target (Group B). In the second stage, the intervention group will be determined according to the results of the KIDMED, the pediatric Mediterranean diet adherence scale. Those in Group B who did not meet the metabolic targets and those with "poor" and "need improvement" KIDMED results will form the intervention group (Group C). Adolescents in Group C will receive a 12-week Mediterranean diet intervention. Information will be collected from participants using questionnaires, scales, and experimental methods. This includes completing the 'Personal Information Form', 'Biochemical Parameters Form', '3-Day Nutrition Questionnaire', 'KIDMED scale', and 'Sensor Data Form'. The obtained data will be analyzed both individually and before-and-after using SPSS 26. The findings are expected to show improvement in OS markers in the intervention group. Improvement in glycemic control markers is also predicted. A decrease in HbA1c levels, a reduction in blood sugar fluctuations, and an increase in the duration of staying within the target range are expected. This study is expected to contribute to the literature by revealing the effects of the Mediterranean diet on oxidative stress and metabolic control parameters in type 1 diabetes. It is anticipated that the findings will support the potential role of dietary approaches with antioxidant properties not only in glycemic control but also in oxidative stress levels and long-term complication risks.

Participants needed: 54
Trial details
Age: 10-18Biological sex: FemaleType: InterventionalSponsor: Istanbul UniversityUpdated: Apr 29, 2026
Eligibility criteria

Ages 10-18 years [+6]

Presence of any acute or chronic disease other than Type 1 Diabetes [+4]

Status: Recruiting

DIEP Flap Breast Reconstruction: Perioperative Biomarkers and Outcomes

Brief Summary This observational study will follow patients who undergo DIEP flap breast reconstruction to better understand a common surgical challenge called ischemia-reperfusion (I/R) injury. I/R injury can happen when a flap has a period without blood flow (ischemia) and then blood flow returns (reperfusion). This process may trigger inflammation and oxidative stress and is associated with fat necrosis or partial flap loss. 1\. What is being studied 1. The investigators will measure inflammation and oxidative stress markers in blood (for example, interleukin-6 \[IL-6\]) from before surgery through the first 72 hours after surgery. 2. These data will help map the normal and abnormal patterns of recovery after surgery and may inform future approaches to monitoring and protecting flap tissue. 3. No experimental drug or device is given to participants in this study. Separate animal studies are developing a near-infrared imaging and antioxidant nanomaterial (Mn/QD-SAC); this is not used in participants here. 2\. Who can take part 1. Women aged 18-70 scheduled for immediate DIEP flap breast reconstruction after breast cancer surgery. 2. Key exclusions include severe heart, liver, or kidney disease; significant clotting problems; active infection or autoimmune disease; long-term use of immunosuppressants/anti-inflammatory drugs; pregnancy or breastfeeding; or other reasons judged by the research team. 3\. What will happen if you join 1. After providing informed consent, participants will have blood drawn at five time points: pre-operative baseline (within 24 hours before surgery) and at 0, 6, 24, and 72 hours after surgery (about 10 mL each time; total \~50 mL). 2. Blood will be processed and stored under secure conditions and tested for inflammation and oxidative stress markers. 3. The investigators will also record routine clinical information from the medical record (such as age, BMI, surgery duration, ischemia time, and clinical assessments of flap outcomes and complications). 4. Participation does not change the participant's clinical care before, during, or after surgery. 4\. Risks and benefits 1. Risks are those of standard blood draws: brief pain, bruising, bleeding, dizziness, and rare infection. 2. There is no direct medical benefit to participants. Results may help improve understanding and future care for patients undergoing flap reconstruction. 5\. Privacy and data protection 1. Samples and data will be coded without names. Identifying information is stored separately with restricted access. 2. Research results are not routinely added to the medical record or returned to participants unless a finding has clear, actionable clinical significance and is approved by the ethics committee. 6\. Time commitment and costs 1. All blood draws occur during the routine hospital stay. There is no additional follow-up required after discharge. 2. There is no cost to participate. 7\. Voluntary participation Joining the study is voluntary. Participants may withdraw at any time without affecting their medical care.

Participants needed: 30
Trial details
Age: 18-70Biological sex: FemaleType: ObservationalSponsor: Hubei Cancer HospitalUpdated: Apr 3, 2026Locations: 1
Eligibility criteria

Female, 18-70 years old. [+2]

Severe cardiac, hepatic, or renal dysfunction or severe coagulopathy (e.g., NYHA... [+4]

Status: Recruiting

Wild Blueberries for Gut, Brain, and Heart Health in Adults With High Blood Pressure

The purpose of the study is to determine the effectiveness of wild blueberries on cardiovascular health, cognitive function, and gut microbiota composition in non-Hispanic Black and White adults with elevated blood pressure.

Participants needed: 40
Trial details
Age: 45-65Biological sex: AllType: InterventionalSponsor: Georgia State UniversityUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Individuals 45-65 years of age [+3]

Allergies to berries [+7]

Status: Recruiting

Wild Blueberries for Gut, Brain, and Cardiometabolic Health in Prediabetes

The goal of this clinical trial is to determine the effectiveness of using a freeze-dried wild blueberry powder on cardiometabolic health, cognitive function, and gut microbiota composition in adult women with prediabetes.

Participants needed: 30
Trial details
Age: 20-65Biological sex: FemaleType: InterventionalSponsor: Georgia State UniversityUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Women aged 20-65 years old [+2]

Allergies to berries [+8]

Status: Recruiting

Oxidative Stress and Inflammatory Biomarkers in Gaucher Disease

The objective of this study is to evaluate oxidative stress and/or inflammation in patients with Gaucher disease type I using a series of biomarkers and correlate with measurements of currently used diagnostic biomarkers.

Participants needed: 34
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: University of MinnesotaUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

All participants must be 18 years or older. [+5]

Medically unstable conditions in any group as determined by the investigators [+5]

Status: Recruiting

Effect of Daily Intake of Gazpacho on Semen Quality and Oxidative Stress

The goal of this clinical trial is to learn whether drinking a daily serving of gazpacho can improve semen quality in men with reduced sperm quality. The study will also examine how this dietary intervention affects oxidative stress and whether it is well tolerated. The main questions this study aims to answer are: * Does daily consumption of gazpacho improve semen quality in men with altered semen parameters? * Does this dietary intervention affect levels of oxidative stress in semen? * Is daily gazpacho intake feasible and well tolerated as part of a Mediterranean diet? Researchers will compare a Mediterranean diet plus daily gazpacho intake with a Mediterranean diet alone to determine whether adding gazpacho provides additional benefits for male reproductive health. Participants will: * Follow a standardized Mediterranean diet for 12 weeks * Drink 330 mL of gazpacho every day or follow the diet without gazpacho * Provide semen samples at the start of the study and after 12 weeks * Complete a short diary to record adherence to the dietary intervention * Be followed for up to 18 months to record reproductive outcomes

Participants needed: 80
Trial details
Age: 18-45Biological sex: MaleType: InterventionalSponsor: GinefivUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Men aged 18 to 45 years [+4]

Use of antioxidant supplements during the three months prior to study start. [+6]

Status: Recruiting

Effect of Ginger Capsules on Inflammation, Oxidative Stress, and Endothelial Function

Randomized, double-blind, parallel, placebo-controlled clinical trial designed and conducted to evaluate the effect of daily consumption of ginger, on parameters related to inflammation, oxidative stress, and endothelial damage in adults with excess adiposity.

Participants needed: 50
Trial details
Age: 23-65Biological sex: AllType: InterventionalSponsor: Ana Mª Garcia MunozUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Male and female participants. [+5]

Presence of acute or chronic diseases not specified in the inclusion criteria. [+8]

Status: Recruiting

Effect of a Ginger-Based Beverage on Inflammation, Oxidative Stress, and Endothelial Function

Randomized, double-blind, parallel, placebo-controlled clinical trial designed and conducted to evaluate the effect of daily consumption of ginger, on parameters related to inflammation, oxidative stress, and endothelial damage in adults with excess adiposity.

Participants needed: 50
Trial details
Age: 23-65Biological sex: AllType: InterventionalSponsor: Javier MarhuendaUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Male and female participants. [+5]

Presence of acute or chronic diseases not specified in the inclusion criteria. [+8]

Status: Recruiting

Environmental Exposure to Heavy Metals, Nanoparticles, and Emergent Contaminants and Risk of Allergic Diseases

The goal of this clinical trial is to collect environmental, bio-humoral, and clinical data derived from patients with allergic contact dermatitis (ACD) and systemic metal allergic syndromes related to the exposure to heavy metals, nanoparticles, and emergent contaminants and from healthy subjects. The main question it aims to answer is: are environmental, bio-humoral, and clinical data derived from patients with ACD and systemic metal allergic syndromes, related to the exposure to heavy metals, nanoparticles, and emergent contaminants, different from ones obtained by healthy subjects? Researchers will compare serum and urine concentration of heavy metals and nanoparticles, patch test to metals, within-breath analysis of oscillometry parameters, serum zonulin, and serum levels of protein oxidation products among patients with systemic allergic syndrome (1st study group), patients with ACD (2nd study group) and healthy subjects (3rd study group). Participants will undergo: * measurement of exposure to heavy metals and nanoparticles including nickel, cobalt, chromium, palladium, molybdenum, aluminium, and copper, through serum and urine measurement of concentration. * Patch test to before mentioned metals. * Within-breath analysis of oscillometry parameters. * Measurement of serum zonulin (related to gastro-intestinal exposure). * Measurement of serum levels of protein oxidation products (as markers of systemic oxidative stress).

Participants needed: 280
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Feb 24, 2026Locations: 2
Eligibility criteria

adult subjects (over 18 years of age). [+4]

Subjects under the age of 18years. [+5]

Status: Recruiting

Chardonnay Marc and Vascular Response

This study aims to obtain data on the potential influence of Vine to Bar product(s) containing Chardonnay marc on cardiometabolic health. These initial studies will inform the design and timing of data collection for future dietary intervention trials that will examine the influence of Chardonnay marc intake on outcomes/biomarkers of both cardiometabolic health and the gut microbiome. This includes collecting data on the potential differences in response to the products based on the unique food matrix for each of the products that will be tested. Moreover, as there is a paucity of data on the influence of cocoa flavanol intake on vascular function beyond 4 hours post intake, the response of the selected outcomes will be assessed after 6 hours of flavanol intake. This is a time point that captures the increased circulating presence of microbial derived flavanol metabolites.

Participants needed: 5
Trial details
Age: 30-50Biological sex: MaleType: InterventionalSponsor: University of California, DavisUpdated: Feb 18, 2026Locations: 1
Eligibility criteria

Screening or Visit 1 Reactive Hyperemia Index (RHI; EndoPAT 2000) < 2.0 [+3]

BMI ≥ 35 kg/m2 [+29]

Status: Recruiting

The ROAR Study: Reactive Oxygen Species and Reproduction

This is a prospective cohort study characterizing follicular fluid and serum levels of oxidative stress in women with various infertility diagnoses undergoing in vitro fertilization, and assessing the relationship of oxidative stress to oocyte competence as determined by embryo development outcomes. Furthermore, we will measure oxidative stress in sperm and correlate the overall oxidative stress within the couple with IVF and pregnancy outcomes of the resultant embryos.

Participants needed: 1,100
Trial details
Age: 18-43Biological sex: AllType: ObservationalSponsor: University of California, San FranciscoUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Female age 18-43 years [+4]

Female partner age 44 or older [+3]