Clinical trials

23

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Condition / disease
Location
Status: Recruiting

Programmed Cell Death Ligand 1 PET/CT in Various PD-L1-Related Disease Patients

To evaluate the potential usefulness of 68Ga/18F-PD-L1 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various PD-L1-related disease patients

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Jun 1, 2026Locations: 2Duration: 7 Days
Eligibility criteria

(i) adult patients (aged 18 years or order); (ii) patients with suspected or new...

(i) patients with non-malignant lesions; (ii) patients with pregnancy; (iii) the...

Status: Recruiting

SNRK & Vascular Endothelial Aging

Cardiovascular diseases pose a serious threat to public health, and their prevalence is on the rise year by year. Vascular aging is an independent risk factor for cardiovascular diseases, and endothelial cell senescence is an early event in vascular aging. Its occurrence can lead to endothelium-dependent vasodilation dysfunction, reduced vascular permeability, and the release of the senescence-associated secretory phenotype (SASP). These vascular pathological changes further damage the vascular media, leading to vascular remodeling and reduced compliance, accelerating the progression of atherosclerosis, and ultimately resulting in cardiovascular diseases such as coronary heart disease and hypertension. Recent research of the investigators has revealed that SNRK, a new member of the AMPK family of cellular energy sensors, plays a key regulatory role in vascular development. Based on this finding, the investigators propose the scientific hypothesis that SNRK responds to both physiological and pathological aging stimuli through differential mechanisms and regulates the process of endothelial cell senescence. In this study, the investigators will explore the correlation between SNRKAS and carotid vascular structure and endothelial function by measuring the levels of the SNRK upstream lncRNA (SNRKAS) in participants' peripheral blood, in conjunction with carotid ultrasound examinations. The findings will provide a solid scientific basis for elucidating new mechanisms underlying the onset and progression of vascular aging and for identifying novel therapeutic targets.

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: May 15, 2026Locations: 1
Eligibility criteria

Aged 18-80 years, with the capacity to make decisions independently or represent... [+2]

Women who are pregnant or may become pregnant; [+4]

Status: Not yet recruiting

FuKe Qianjin Capsule Plus Antibiotics for Chronic Endometritis

This randomized, double-blind, single-dummy, multicenter clinical study, led by Principal Investigator Xue Fengxia at Tianjin Medical University General Hospital (sponsor and primary trial institution) and funded by Zhuzhou Qianjin Pharmaceutical Co., Ltd., evaluates the safety and efficacy of FuKe Qianjin Capsules combined with standard antibiotic therapy for chronic endometritis (CE) in women aged 20-40 years. CE, a common gynecological inflammation marked by uterine plasma cell infiltration from bacterial infection, is linked to infertility, repeated implantation failure (RIF), and recurrent miscarriage (RM); it is often underdiagnosed due to non-specific symptoms, and first-line doxycycline therapy is limited by antibiotic resistance and high recurrence. FuKe Qianjin Capsules, a nationally recognized Chinese herbal medicine for gynecological inflammations, align with traditional Chinese medicine (TCM) treatment principles for CE (damp-heat stasis with qi and blood deficiency) and reduce antibiotic resistance per domestic research. Approximately 300 eligible participants (confirmed CE via hysteroscopy/pathology, matching TCM syndrome, regular menstrual cycles, informed consent) will be enrolled across 10-15 Chinese centers, with exclusion for acute infections, gynecological malignancies/ severe uterine lesions, organ dysfunction, uncontrolled systemic diseases, pregnancy/lactation, drug hypersensitivity, or recent trial participation. All receive 14 days of oral doxycycline (100mg twice daily) and are randomized 1:1 to two double-blind groups (150 each): Experimental Group (56 days of FuKe Qianjin Capsules, 0.4g/capsule, 2 capsules three times daily) or Control Group (56 days of matched capsule placebo). The study includes a 28-day screening period, 56-day treatment phase, and 6-month post-treatment follow-up (in-person visits at Day 28±5/56±7; telephone/outpatient follow-up at 3/6 months). Efficacy assessments (hysteroscopy, TCM scoring, ultrasound), safety monitoring (vital signs, blood work, pregnancy testing), adverse event recording, and medication adherence checks occur at all visits, with ultrasound-confirmed clinical pregnancy rate as the key post-treatment outcome. The team monitors known drug adverse effects (mild gastrointestinal/skin/neurological symptoms for the capsules; gastrointestinal/photosensitivity/rare liver/blood issues for doxycycline) and hysteroscopy risks (mild bleeding, rare perforation), with emergency protocols in place. Participants may withdraw voluntarily at any time with no impact on regular care; all data/specimens are confidential, de-identified, and used only for study research (no commercial use). Overseen by the hospital's Institutional Ethics Committee and compliant with national research standards, the study's primary goal is to confirm the combined regimen's superior safety and efficacy over antibiotic monotherapy for CE, as well as its ability to improve reproductive outcomes and reduce recurrence. A positive result will establish this integrated Chinese-Western medicine approach as an evidence-based CE treatment, reducing antibiotic resistance and enhancing reproductive health for affected women, especially those with infertility, RIF, or recurrent miscarriage.

Participants needed: 300
Trial details
Phase: Phase 4Age: 20-40Biological sex: FemaleType: InterventionalSponsor: Tianjin Medical UniversityUpdated: Mar 20, 2026Locations: 1
Eligibility criteria

Age range: 20 years old ≤ age ≤ 40 years old; [+4]

Patients with concurrent acute genital tract and pelvic infections, etc. [+11]

Status: Recruiting

ALI & Pulmonary HA Deposition After SAH

Acute lung injury is a common complication of subarachnoid hematoma (SAH), and a significant risk factor for death in patients with SAH. Unlike neurogenic pulmonary edema and pneumonia following brain injury, the clinical causes of pulmonary injury after SAH are not intracranial hypertension or pulmonary infection. Its occurrence is influenced by the release of catecholamines, the regulatory function of the hypothalamic-pituitary-adrenal (HPA) axis and systemic inflammatory response, but the specific mechanisms are still unclear. Therefore, delving into the pathological mechanisms of SAH-induced lung injury and developing therapeutic strategies based on the findings is of great importance to improve the prognosis of patients. Abnormal accumulation of hyaluronic acid in the lungs has been reported to be closely related to the pathological progression of various pulmonary injury diseases, such as chest trauma, pulmonary infection and chronic obstructive pulmonary disease. From this, the present research is aimed to explore the levels and dynamic changes of hyaluronic acid in the bronchoalveolar lavage fluid and blood of patients with acute lung injury following SAH, and to analyze its correlation with the prognosis of pulmonary complications, thereby providing assistance for the clinical diagnosis and treatment of SAH.

Participants needed: 24
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Mar 18, 2026Locations: 1
Eligibility criteria

Age between 18 and 80 years old with independent behavior ability or authorized... [+3]

Pregnant or lactating women. [+4]

Status: Not yet recruiting

Effectiveness of Xuanfei Jiangzhuo Decoction for Influenza-Induced AECOPD

The goal of this observational study is to learn if a traditional Chinese herbal medicine (Xuanfei Jiangzhuo Decoction) works to help older adults recover from a COPD flare-up caused by the flu (influenza virus). The main questions it aims to answer are: Does the herbal medicine help participants feel better and recover faster? Does it lower the chance of getting a second infection from bacteria? Is the herbal medicine safe to use? Researchers will compare participants who choose to take the herbal medicine along with their standard flu treatment (Oseltamivir or Baloxavir) to participants who only take the standard flu treatment (Oseltamivir or Baloxavir). Participants will: Take the herbal medicine (a liquid drink) twice a day for 5 days, or just take their standard flu medicine for 5 days. Visit the clinic 4 times over 28 days for checkups and tests. Provide blood and stool samples to help researchers understand how the medicine affects the body and gut health. Answer simple questions about their cough, breathing, and energy levels.

Participants needed: 300
Trial details
Age: 60+Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Mar 12, 2026Locations: 1Duration: 28 Days
Eligibility criteria

Diagnosed with Influenza-induced AECOPD according to the Global Strategy for the... [+2]

Known allergy or hypersensitivity to any component of the study medications. [+5]

Status: Recruiting

Alpha-Synuclein PET/CT in Various α-Syn-Related Disease

To evaluate the potential usefulness of 18F-FIAT-2, 18F-C05-05, 18F-SPAL-T-06 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various α-Syn-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Jan 29, 2026Locations: 2Duration: 7 Days
Eligibility criteria

(i) adult patients (aged 18 years or order); (ii) patients with suspected or new...

(i) patients with none PD syndrome; (ii) patients with pregnancy; (iii) the inab...

Status: Recruiting

Amino Acid Transporter System PET/CT Imaging in AATS-Related Diseases

To evaluate the potential usefulness of 11C/18F-MET/FET positron emission tomography/ computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various amino acid transporter system (AATS)-related disease patients.

Participants needed: 500
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Jan 30, 2026Locations: 2Duration: 7 Days
Eligibility criteria

adult patients (aged 18 years or order); [+3]

patients with non-malignant lesions; [+2]

Status: Recruiting

[18F]NIDF PET Imaging in Tau-related Diseases

In the field of diagnosing brain neurodegenerative diseases, it is now a well-established practice to inject positron-emitting tracers into the human body. These tracers bind to specific target proteins, allowing their distribution to be visualized via PET imaging. Currently, several research groups worldwide are engaged in developing and clinically validating their own tau imaging agents. This clinical research project aims to visualize abnormal tau pathology in the living human brain using \[18F\]NIDF PET imaging. \[18F\]NIDF is a 2-arene-azaindole-based tracer that offers stronger binding affinity to tau neurofibrillary tangles and reduced non-specific/off-target binding compared to existing tau-PET imaging agents. The study primarily focuses on evaluating the safety and diagnostic efficacy of \[18F\]NIDF PET imaging in human subjects.

Participants needed: 20
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Dec 29, 2025Locations: 2Duration: 7 Days
Eligibility criteria

Between 18 and 90 years old; [+4]

Has allergy to [18F]NIDF or any of its excipients; [+6]

Status: Recruiting

[18F]FT8 PET Imaging in Immunoglobulin Light Chain Amyloidosis

\[18F\]FT8, a derivative of 1-(4-pyridyl)-4-piperazinyl arene (\[18F\]TPZA), exhibits high affinity for AL amyloid in myocardial tissue sections and shows no significant binding to transthyretin amyloid. By comparing its diagnostic performance against established clinical methods, including echocardiography, contrast-enhanced MRI, and relevant laboratory tests, this study aims to establish \[18F\]FT8 as the basis for a robust PET protocol for the direct visualization and differential diagnosis of AL amyloidosis . The study preimarily evaluates the safety and diagnostic efficacy of \[18F\]FT8 PET imaging in human subjects.

Participants needed: 25
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Nov 18, 2025Locations: 2Duration: 7 Days
Eligibility criteria

Subject Recruitment Participants will be recruited from outpatients and/or inpat... [+4]

Confirmed non-cardiac amyloidosis or other non-amyloid cardiac pathologies that... [+7]

Status: Recruiting

Pan-Amyloid PET/CT in Various Amyloid-Related Disease

To evaluate the potential usefulness of 18F-92/AV45/TPZA/FT8, 11C-PIB positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various Pan-Amyloid-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Aug 19, 2025Locations: 2Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

Prostate Specific Membrane Antigen PET/CT Imaging in PSMA-Related Disease Patients

To evaluate the potential usefulness of 68Ga/18F-PSMA/PSFA positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various PSMA-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Aug 11, 2025Locations: 2Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

Beta Amyloid PET/CT in Various Aβ-Related Disease

To evaluate the potential usefulness of 18F-92/AV45, 11C-PIB positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various Tau-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Jun 4, 2025Locations: 3Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

Hydroxyephedrine PET/CT in Sympathetic Nervous System Disease

To evaluate the potential usefulness of 11C/18F-HED positron emission tomography/ computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various Tau-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Apr 30, 2025Locations: 1Duration: 7 Days
Eligibility criteria

(i) adult patients (aged 18 years or order); (ii) patients with suspected or new...

(i) patients with non-malignant lesions; (ii) patients with pregnancy; (iii) the...

Status: Recruiting

Translocator Protein PET/CT in Various TSPO-Related Disease

To evaluate the potential usefulness of 18F-DPA714/FDPA positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various TSPO-related disease patients.

Participants needed: 200
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Feb 11, 2025Locations: 2Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

Glucagon-like Peptide-1 Receptor PET/CT in GLP-1R Related Disease

To evaluate the potential usefulness of 68Ga/18F-Exendin 4 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various GLP-1R-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Feb 11, 2025Locations: 1Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

Somatostatin Receptor PET/CT in SSTR-Related Disease Patients

To evaluate the potential usefulness of 68Ga/18F-TATE/JR11/LM3 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various SSTR-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Feb 11, 2025Locations: 1Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

Chemokine Receptor 4 PET/CT Imaging of CXCR4-Related Diseases

To evaluate the potential usefulness of 68Ga/18F-Pentixafor/Pentixather positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various CXCR4-related disease patients.

Participants needed: 200
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Tianjin Medical UniversityUpdated: Feb 11, 2025Locations: 1
Eligibility criteria

suspected or confirmed untreated Lymphoproliferative and other CXCR4-related dis... [+2]

pregnancy [+2]

Status: Recruiting

Tau PET/CT in Various Tau-Related Disease Patients

To evaluate the potential usefulness of 18F-S16/T807 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various Tau-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Feb 11, 2025Locations: 2Duration: 7 Days
Eligibility criteria

Not listed

Status: Recruiting

FAPI PET/CT in Various FAP-Related Disease Patients

To evaluate the potential usefulness of 68Ga/18F-FAPI positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various FAP-related disease patients.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Feb 11, 2025Locations: 1Duration: 7 Days
Eligibility criteria

(i) adult patients (aged 18 years or order); (ii) patients with suspected or new...

(i) patients with non-malignant lesions; (ii) patients with pregnancy; (iii) the...

Status: Recruiting

A Study of YUTIQ® 0.18 mg Intravitreal Implant for the Management of Chronic Non-infectious Uveitis

This project is designed to evaluate the efficacy of YUTIQ® 0.18 mg intravitreal implant for the management of chronic non-infectious uveitis.

Participants needed: 15
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

Male or female in good general health at 18 to 70 years of age. [+3]

Subject with corneal or lens opacity that precludes visualization of the fundus... [+8]

Status: Recruiting

A Study of Adalimumab in Acute Vogt-Koyanagi-Harada Disease

This project is designed to test the hypothesis that adalimumab is clinically useful for patients with acuta Vogt-Koyanagi-Harada disease

Participants needed: 15
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

Subject is 18 to 70 years of age. [+3]

Subject with confirmed or suspected infectious uveitis, including but not limite... [+5]

Status: Recruiting

Clinical Study of High Concentration Ganciclovir Eye Drops in the Treatment of Cytomegalovirus Retinitis

Clinical study of high concentration ganciclovir eye drops in the treatment of cytomegalovirus retinitis

Participants needed: 15
Trial details
Phase: Early Phase 1Age: 2-80Biological sex: AllType: InterventionalSponsor: Tianjin Medical UniversityUpdated: Jun 23, 2023Locations: 1
Eligibility criteria

Patients voluntarily participate in studies and sign informed consent forms [+2]

Eye condition [+6]

Status: Not yet recruiting

Displacement of Iodine Balance Value During Pregnancy and the Mechanism of Breast Iodine Homeostasis During Lactation

In order to solve the bottleneck problems of"zero balance displacement"and"large variation of breastmilk"in the study of iodine EAR of pregnant women, lactating women and infants, firstly, this study intends to clarify the rate of metabolism and distribution of iodine during pregnancy by 125I tracer, SPECT/CT in vivo small animal imaging and γ counting study. Then, the iodine balance study in rats was conducted to verify the degree of "zero balance value displacement"caused by the difference of iodine absorption and store in different organs and tissues under different iodine exposure levels, so as to determine the iodine selection conditions of subjects in the population experiment. To determine the EAR of pregnant women by optimizing the population iodine balance experiment. Secondly, we proposed to study the regulatory mechanism of NIS and Pendrin in the mammary gland of lactating rats under different iodine nutrition levels to clarify the range of breastmilk iodine compensation. Mammary cell experiments intend to clarify the mutual regulations of iodine nutrition, oestrogen, and NIS and Pendrin. Based on the results of animal and cellular experiments, and the effect of genetic, oestrogen and iodine status were considered, a cross-sectional study of lactating women was conducted to determine the normal reference range of breastmilk iodine after screening out the people with abnormal indicators. This study will solve the bottleneck problems and difficulties in the iodine RNI research for pregnant women, lactating women and infants, found the iodine nutritional compensatory mechanism under special physiology, and provide the scientific basis for obtaining the accurate EAR basic data and the revision of iodine DRIs.

Participants needed: 1,200
Trial details
Age: 1-40Biological sex: FemaleType: ObservationalSponsor: Tianjin Medical UniversityUpdated: Feb 16, 2023Locations: 2
Eligibility criteria

Aged 18-40, who have lived in the area for ≥5 year; [+5]

Smoking or drinking; [+4]