Clinical trials

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Condition / disease
Location
Status: Recruiting

Investigation of the Individual Fatigue Response During Blood Flow Restriction Training

The aim of the present pilot study is to investigate the feasibility of an exercise pressure response approach for assessing physiological strain during BFR training in a clinically supervised setting. Patients undergoing rehabilitation following total knee arthroplasty (TKA) will be included. The results are intended to contribute to an improved evaluation of load management during BFR training.

Participants needed: 20
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Elective TKA caused by osteoarthritis of the knee [+2]

Open Wounds [+2]

Status: Recruiting

Blood Flow Restriction Training in Acute Geriatric Rehabilitation

Background: Older adults have a reduced ability to build and maintain muscle mass due to age-related changes in the muscular system. The resulting sarcopenia can lead to a number of health problems and limitations, such as an increased risk of falling and reduced mobility, which can affect quality of life and increase the risk of disease. To increase muscle mass and strength, high-intensity resistance training with loads of 70 to 85% of the repetition maximum (1RM) is recommended. However, this type of training poses a major challenge in the rehabilitation sector, as there is also an increased risk of injury due to physical limitations in old age. According to current research, low-intensity occlusion training could therefore represent a safe and effective training alternative. The aim of this study is therefore to examine the feasibility and effects of blood flow restriction training (BFR) on general health in older adults in a rehabilitative setting.

Participants needed: 60
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: May 14, 2026Locations: 1
Eligibility criteria

Adults >65 years with a two week hospitalized acute rehabilitation after a fract...

Sickle Cell Anemia [+1]

Status: Recruiting

Immunochemotherapy, Surgery or Chemoradiation, and Durvalumab for Stage IIIA/B NSCLC

The hypothesis of the study is that induction immunochemotherapy, followed by surgery or chemoradiation and consolidation Durvalumab immunotherapy, can significantly improve event-free survival in patients with resectable or borderline resectable NSCLC at stage IIIA/B compared to existing treatment methods.

Participants needed: 176
Trial details
Phase: Phase 2Age: 18-74Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Jan 27, 2026Locations: 5
Eligibility criteria

IIIA: one or more lymph node levels involved at EBUS/mediastinoscopy T1/T2 N2. [+4]

Must not have experienced a toxicity that led to permanent discontinuation of pr... [+6]

Status: Recruiting

Slowing Cognitive Decline in Alpha-synucleinopathies by Enhancing Physical Activity

α-Synucleinopathies, including Parkinson's disease and dementia with Lewy bodies, are the second most common neurodegenerative diseases. In addition to progressive motor deterioration, cognitive decline is a key element of the non-motor symptom complex of these diseases. Isolated rapid eye movement (REM) sleep behavior disorder (iRBD) indicates an early stage of α-synucleinopathies, even before relevant motor or cognitive disorders are present. Therapeutic interventions in individuals with iRBD therefore have great preventive potential. In particular, increasing physical activity could have a relevant effect on neurodegenerative processes, including the preservation of cognitive functions. The aim of the study is therefore to investigate the effects of increased physical activity in everyday life on cognitive functions in individuals with iRBD. In this randomized, double-blind, actively controlled study, an increase in physical activity will be implemented over a period of one year with the help of a motivational smartphone application. The intervention and control conditions are the same as those used in the Slow-SPEED trials, making the connection between the trials concrete. The primary outcome parameter is the change in cognitive performance in a neuropsychological test battery over one year. Eighty individuals with iRBD and 50 age- and gender-matched individuals are being recruited at the University Hospital Bonn and the "Deutsches Zentrum für Neurodegenerative Erkrankungen" (DZNE) Bonn (German branch only). In addition to classic neuropsychological tests as the primary endpoint, magnetic resonance imaging (MRI) and blood-based markers of brain aging are being examined as secondary endpoints. This study is in close collaboration with the Slow-SPEED study (https://clinicaltrials.gov/study/NCT06993142). In addition, selected data from three separate trials-Alpha-Fit, Slow-SPEED-NL, and a sister trial in Austria currently in preparation-are planned to be synthesized into a meta-analysis.

Participants needed: 130
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Jan 16, 2026Locations: 1
Eligibility criteria

Age: 50-80 years [+14]

Relevant cardiovascular diseases [+8]

Status: Recruiting

Analysis of Pharmacological Aspects Regarding Infection Free Survival After Surgical Treatment of a Periprosthetic Hip Infection: a Microdialysis Study

This study aims to use the technique of microdialysis to analyse the intraarticular space of the hip joint after removal of a periprosthetic joint infection affected endoprosthesis and implantation of an antibiotic-containing cement spacer over the entire period of the first hospitalization (usually 14 days) to closely monitor pharmacological and immunological aspects. In detail, antibiotic concentrations in the joint cavity and systemic circulation will be assessed according to reinfection rates, infection-free survival and fucntional outcome over a 12-month folluw-up period.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

clinical indication for two-stage revision of hip PJI [+3]

- known allergies to antibiotics gentamicin and vancomycin used within the space...

Status: Recruiting

Analysis of Pharmacological Aspects Regarding Infection Free Survival After Surgical Treatment of a Periprosthetic Knee Infection: a Microdialysis Study

This study aims to use the technique of microdialysis to analyse the intraarticular space of the knee joint after removal of a periprosthetic joint infection affected endoprosthesis and implantation of an antibiotic-containing cement spacer over the entire period of the first hospitalization (usually 14 days) to closely monitor pharmacological and immunological aspects. In detail, antibiotic concentrations in the joint cavity and systemic circulation will be assessed according to reinfection rates, infection-free survival and fucntional outcome over a 12-month folluw-up period.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

clinical indication for two-stage revision of knee PJI [+3]

known allergies to antibiotics gentamicin and vancomycin used within the spacer

Status: Recruiting

Impact of Rehabilitation Therapy Using Strength and Blood Flow Restriction Training on Muscular Fitness and Regeneration After Elective Hip Replacement

In the present project, the framework conditions of outpatient rehabilitation at the Bonn Center for Outpatient Rehabilitation will now be used to prove whether sports science-controlled strength and BFR training has a similar effect in the postoperative rehabilitation phase. Strength and BFR training in medical training therapy complements daily exercise therapy in order to ensure implementation in the guideline-based rehabilitation process. . The interventions are carried out as part of the exercise therapy units in outpatient rehabilitation ETM01 following the RTS hip and knee TEP basis KTL 2020.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Dec 8, 2025Locations: 1
Eligibility criteria

Ability for Rehabilitation [+1]

Sickle Cell Anemia [+2]

Status: Recruiting

Clinical-randomized Trial of the Effect of Rehabilitation Therapy Using Strength and Blood Flow Restriction Training on Muscular Fitness and Regeneration After Anterior Cruciate Ligament Reconstruction

With the intention of improving rehabilitation after anterior cruciate ligament reconstruction, the present project investigates the influence of a targeted strength and blood flow restriction training intervention (BFR training) on the regeneration of muscle mass, strength and functionality of the knee joint. BFR training is characterized by the combination of external venous vascular occlusion with light strength training and still enables users to achieve gains in muscle mass and strength that are comparable to training with high mechanical loads. The positive effects of BFR training in the course of knee arthroplasty have already been demonstrated by our working group as a prehabilitative approach, i.e. as a training intervention prior to surgery. In the present project, the framework conditions of outpatient rehabilitation at the Bonn Center for Outpatient Rehabilitation will now be used to prove whether sports science-controlled strength and BFR training has a similar effect in the postoperative rehabilitation phase. The interventions are carried out as part of the exercise therapy units in outpatient rehabilitation ETM01 in accordance with the S2k guideline on anterior cruciate ligament rupture. Strength and BFR training in medical training therapy supplements the daily exercise therapy to ensure implementation in the rehabilitation process in line with the guidelines.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Dec 8, 2025Locations: 1
Eligibility criteria

ACL reconstruction [+1]

Sickle Cell anemia [+2]

Status: Recruiting

Brain and Voice Signatures in Teachers

Primary muscle tension dysphonia voice disorder with symptoms of vocal strain and vocal fatigue is common and can have a significant negative impact on quality of Life. Yet, primary muscle tension dysphonia's causes are unknown precluding precise diagnostic classification. Stress and personality are thought to play a role and thus, the project aims to determine the practical and clinical effect of stress on the control of voice and speech in the brain. Participants are female early career teachers and student teachers with symptoms of vocal fatigue, as well as control participants without vocal fatigue, who perform speech tasks on two different occasions. Neural (imaging of brain), psychobiological (saliva, personality), and voice and speech (muscle activity of voice muscles on the neck with surface sensors, audio recordings) data will compare reactivity patterns of teachers who are stressresponders with those who are nonresponders as well as control participants. The central hypothesis is that voice box stress responders have heightened emotion-motor activations involving the emotional voice production pathway, which correlate with changes in voice muscle activity in the anterior neck. The results will provide fundamentally missing data in our understanding of the role of stress in vocal complaints and will yield new insights about the neural underpinnings of primary muscle tension dysphonia. The study findings will have a significant impact on how clinicians identify so-called laryngoresponders to help them prevent voice disorders.

Participants needed: 100
Trial details
Age: 21-39Biological sex: FemaleType: InterventionalSponsor: University Hospital, BonnUpdated: Aug 27, 2025Locations: 1
Eligibility criteria

Lefthandedness [+13]

Status: Recruiting

Progression Assessment of PXE-associated Alterations

This monocentric clinical observational study at the University Eye Hospital Bonn investigates the natural history and structural consequences of a diseased Bruch's membrane (BrM) in Pseudoxanthoma elasticum (PXE). The study includes four main objectives: 1. Direct Bruch's Membrane Alterations: Longitudinal analysis of BrM reflectivity using high-resolution OCT to assess correlations with disease progression 2. Choriocapillaris Flow Deficits: Evaluation of choriocapillaris (CC) perfusion in relation to BrM calcification, aiming to clarify whether CC deficits precede or result from BrM changes 3. Retinal Atrophy Progression: Monitoring the development and expansion of retinal atrophic areas over two years, including correlations with specific features like reticular pseudodrusen and hyperreflective spots 4. Genotype-Phenotype Correlation: Analysis of different ABCC6 gene mutations to identify correlations with imaging features and disease severity, potentially guiding future personalized therapeutic strategies The study will recruit 100 PXE patients and 100 controls, with data collection over 10 years. It involves non-invasive imaging and blood sampling. No direct benefit is expected for participants, but the findings may inform future clinical trials and improve patient counseling.

Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Jul 2, 2025Locations: 1
Eligibility criteria

PXE based on the criteria of Plomp et al. [+2]

Any confounding ocular disease not associated with PXE [+1]

Status: Recruiting

Anterior Temporal Lobectomy in Temporal Glioblastoma

The ATLAS/NOA-29 trial is a prospective, multicenter, phase III randomized controlled study evaluating whether anterior temporal lobectomy (ATL), a standardized resection technique adapted from epilepsy surgery, improves clinical outcomes in patients with newly diagnosed glioblastoma of the anterior temporal lobe compared to conventional gross-total resection (GTR). The rationale is based on the concept of glioblastoma as a diffusely connected tumor network, with infiltrative spread extending beyond MRI-detectable tumor margins. ATL offers a reproducible supramarginal resection approach within anatomical boundaries that are routinely respected in epilepsy surgery. Patients are randomized intraoperatively in a 1:1 ratio following histopathological confirmation via intraoperative frozen section procedure. The trial's primary objective is to demonstrate superiority of ATL in overall survival (OS), while confirming non-inferiority in health-related quality of life (QoL), measured by the global health status scale of the European Organisation for Research and Treatment of Cancer (EORTC) - Quality of Life Questionnaire Core 30 (QLQ-C30). Secondary outcomes include progression-free survival (PFS), seizure control, neurocognitive functioning, and longitudinal assessments of selected EORTC QLQ-C30 and BN20 domains. A total of 178 patients will be enrolled over three years, with a minimum follow-up of three years. An interim safety analysis after inclusion of 57 patients will assess functional outcome differences using the modified Rankin Scale (mRS) at 6 months postoperatively. The study is powered (\>80%) to detect a survival benefit assuming a median OS increase from 17 to 27.5 months. If proven superior to GTR, ATL could emerge as the preferred surgical strategy for isolated temporal lobe glioblastoma, offering robust evidence in favor of extending supramarginal resection principles to the broader context of glioblastoma care.

Participants needed: 178
Trial details
Phase: Phase 3Age: 18-74Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Jun 13, 2025Locations: 1
Eligibility criteria

Suspected glioblastoma with contrast-enhancement in preoperative MRI [+20]

Status: Recruiting

Impact of Different Perioperative Tourniquets on Blood Loss and Surgeon Satisfaction in Total Knee Arthroplasty

The present study investigates the impact of two different perioperative tourniquets with different closing features on operative blood los, surgical field quality and surgeon satisfaction.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Apr 27, 2025Locations: 1
Eligibility criteria

Inidication for a Total Knee Arthroplasty [+1]

Open Wounds of the lower extremities [+1]

Status: Recruiting

Acute Effects of Physical Exercise in Patients with Borderline Personality Disorder

The aim of the proposed project is to investigate the effects of a single session of physical exercise on stress regulation, cognitive and emotional functioning, and associated neurophysiological processes (saliva and blood samples) in patients with borderline personality disorder. A further aim is to identify the optimal exercise intensity (moderate vs. high intensity). The investigatiors expect that acute exercise will lead to positive effects on behavioral and biomarker level.

Participants needed: 120
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Dec 11, 2024Locations: 1
Eligibility criteria

estimated verbal intelligence quotient >80 (MWT-B; Lehrl 2005) [+1]

neurological disorders [+5]

Status: Recruiting

AI-POD Clinical Validation Study for Obese Patients

The study is aimed at patients who suffer from severe obesity and receive a computerised tomography (CT) scan of the heart. A total of 1200 patients across Europe are to take part in the study. It is a multi-centre, controlled, open, randomised study. As part of the study, a citizen app will be installed on a smartphone for randomly selected study participants. A fitness tracker will also be issued so that certain parameters, such as heart rate and daily number of steps, can be recorded.

Participants needed: 1,200
Trial details
Age: 45+Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Sep 19, 2024Locations: 6
Eligibility criteria

Age greater than or equal to 45 years at the time of signing informed consent [+3]

Any of the following CV conditions within 2 months prior to study inclusion: myo... [+11]

Status: Recruiting

Placebo Optimization of the Presurgical Long-term Video-EEG Monitoring

The notion of genuine placebo effects on epileptic seizure events (i.e., effects beyond methodological study artifacts) is incompatible with the standard model of epilepsy seizure genesis. In this single-blind controlled study, the effectiveness of a covered placebo on (1) the timing of the occurrence of a first epileptic seizure ("seizure pill") versus (2) the subjective well-being ("comfort pill") during pre-surgical video-EEG monitoring will be examined. It is hypothesized that a placebo effect on subjective well-being can be demonstrated, but that epileptic seizure events are not influenced by placebo.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, BonnUpdated: Jun 10, 2024Locations: 1
Eligibility criteria

eligibility for presurgical epilepsy diagnostics

inclusion criterion implies all exclusion criteria for this procedure [+2]

Status: Recruiting

Prevalence of Synovitis in Patients With Haemophilia A

The aim of this study is to evaluate the prevalence of synovitis in adult patients with haemophilia A.

Participants needed: 300
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: University Hospital, BonnUpdated: Apr 16, 2024Locations: 1
Eligibility criteria

Participants (≥ 18 years old) suffering from moderate or severe haemophilia A, a... [+2]

Patients suffering from other bleeding disorders conflicting with the research q... [+1]

Status: Recruiting

Predicting Acute-on-Chronic Liver Failure After Surgical Intervention in Chronic Liver Disease

Prospective, observational study to define precipitants and predictors of development of Acute-on-Chronic Liver Failure (ACLF) after surgical interventions, allowing to develop a risk stratification for elective procedures in cirrhotic patients. As well as identifying molecular mechanisms of post-interventional ACLF and thus preparing the ground for development of new therapeutic approaches.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: May 18, 2022Locations: 1
Eligibility criteria

Male or female adult (≥18 years) patient [+7]

Pregnant or lactating females [+7]

Status: Recruiting

Non-invasive Evaluation of the Predictive Value of CEUS and SWE in ACLF, Renal Failure and Hepatorenal Syndrome

Evaluation of non-invasive prognostic parameters in patients developing ACLF and renal failure in patients receiving and not receiving transjugular intrahepatic portosystemic shunt (TIPS). Patients are cared according to the local standardized follow up program. Clinical and laboratory data from standard patient care are evaluated for potential prognostic value.

Participants needed: 1,000
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: May 18, 2022Locations: 1
Eligibility criteria

All patients with portal hypertension and kidney failure

no consent, no kidney failure, no portal hypertension

Status: Recruiting

Non-Invasive Characterization of Focal Liver Lesions in Liver Cirrhosis

This study aims to analyze non-invasive characterization focal liver lesions in patients with liver cirrhosis. The diagnostic accuracy and predictive value of non-invasive methods is studied.

Participants needed: 200
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: May 18, 2022Locations: 1
Eligibility criteria

all patients with focal liver lesions and liver cirrhosis

no consent [+1]

Status: Recruiting

Immunophenotyping in Patients With Osteoporosis

In addition to a medical history and clinical examination, the diagnosis of osteoporosis includes the measurement of bone surface density by means of dual X-ray absorptiometry (DXA). In addition, blood tests are performed for certain parameters, such as vitamin D, calcium, phosphate and C-reactive protein. In order to optimize osteoporosis diagnostics, the development of further specific methods is required. The modulation of the immune system seems promising in this respect, since osteoporosis is based on an inflammatory reaction. Various regulatory markers of the innate and acquired immune system, which seem to be relevant in the development of the disease, have already been detected in osteoporosis patients. This study may help to gain new insights into disease-associated immunoregulatory markers that could revolutionize both the diagnosis and therapy of osteoporosis in the long term. By means of a simple blood test, patients could be diagnosed early and without additional radiation exposure, and effective therapy options could be developed.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Nov 24, 2021Locations: 1
Eligibility criteria

Adult patients (≥ 18 years) diagnosed with osteoporosis. [+1]

Patients without diagnosed osteoporosis [+3]

Status: Recruiting

Non-invasive Evaluation Program for TIPS and Follow Up Network 2 (NEPTUN2)

Evaluation of non-invasive prognostic parameters in patients receiving transjugular intrahepatic portosystemic shunt (TIPS) for complications of portal hypertension. Patients are cared according to the local standardized follow up program. Clinical and laboratory data from standard patient care are evaluated for potential prognostic value.

Participants needed: 1,000
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Oct 5, 2021Locations: 1
Eligibility criteria

Insertion of TIPS according to guidelines

Contraindication for TIPS

Status: Recruiting

Vascular Liver Disease Evaluation, Follow Up and Non-Invasive Diagnostics Program

Background Vascular liver disorders (VALDI) are rare diseases, for which knowledge on risk factors, appropriate methods of diagnosis, effect of therapy and prognosis still need to be improved. Aim of the study This project aims to study risk factors, methods of detection, therapy and prognosis in order to elaborate and disseminate updated recommendations for the optimal management of patients with VALDI. Design of the study Data on patients will be collected from baseline (the date of diagnosis) up to 3 years. During this period, data on clinical condition, laboratory results, diagnostic tests, interventions and outcome will be collected anonymously using standardised review of medical charts by one special trained investigator. Only patients with VALDI are eligible to participate.

Participants needed: 500
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Oct 5, 2021Locations: 1
Eligibility criteria

all patients with vascular liver disease

patients without vascular liver disease

Status: Recruiting

Skeletal Muscle Parameters of Liver Cirrhosis in Non-invasive Imaging and Outcome

The principal aim of this study is to analyse L3-SMI (skeletal muscle index) in a cohort of patients with decompensated liver cirrhosis and TIPS (transjugular intrahepatic portosystemic shunt), and compare the prognostic power with TPMT (transverse psoas muscle thickness). Furthermore, the role of myosteatosis, determined in CT by L3-SMI, MRI and ultrasound will be studied.

Participants needed: 400
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: University Hospital, BonnUpdated: Oct 5, 2021Locations: 3
Eligibility criteria

liver cirrhosis of any etiology [+1]

HCC or any malignant disease