Clinical trials

6

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Community-based Prospective Cohort Study on Metabolic Dysfunction-Associated Fatty Liver Disease in Older Adults: From Metabolic Trajectories to Extrahepatic Outcomes

To establish a cohort of elderly fatty liver disease based on the community medical examination population. Through the large-scale cohort study, the risk factors affecting fatty liver in the elderly will be explored in depth from the aspects of lifestyle, environment and genetics, the development pattern and mechanism of fatty liver in the elderly will be analysed, and the health risk assessment system and Chinese standard for fatty liver in the elderly covering cardiovascular risk, risk of hepatic fibrosis and risk of sarcopenia will be established, so as to provide the scientific basis for the precise intervention of fatty liver in the elderly in China.

Participants needed: 20,000
Trial details
Age: 65-100Biological sex: AllType: ObservationalSponsor: The Affiliated Hospital of Hangzhou Normal UniversityUpdated: Jun 1, 2026Locations: 1Duration: 2 Years
Eligibility criteria

① Elderly people aged ≥65 years among permanent residents (living for more than... [+1]

①Major disability, mental illness, major wasting disease, severe cardiac, pulmon... [+1]

Status: Not yet recruiting

Personalized Transcranial Magnetic Stimulation (TMS) for Metabolic Dysfunction and Alcohol-Related Liver Disease

The goal of this clinical trial is to learn if repetitive Transcranial Magnetic Stimulation (rTMS), a non-invasive brain stimulation technique, works to treat Metabolic dysfunction-associated and alcohol-associated liver disease (MetALD). The main questions it aims to answer are: * Can rTMS effectively treat MetALD? * Is an individualized, precision-targeted rTMS approach more effective than the standard rTMS method? * What changes in brain activity are associated with the treatment? Researchers will compare three different types of stimulation: * Group A: Individualized rTMS targeting a deep brain reward area (the Nucleus Accumbens) based on each participant's brain scan (fMRI). * Group B: Standard rTMS applied using the traditional "5 cm" rule for positioning. * Group C: Sham (placebo) rTMS, which mimics the procedure but delivers no significant magnetic stimulation. Participants will: * Be randomly assigned to one of the three groups (A, B, or C). * Undergo an MRI brain scan before starting treatment. * Receive a total of 20 rTMS sessions, completing at least 4 sessions per week. * Have additional MRI scans and clinical assessments halfway through and immediately after the treatment course. * Attend follow-up visits at 1, 3, and 6 months after treatment completion to assess long-term effects.

Participants needed: 105
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: The Affiliated Hospital of Hangzhou Normal UniversityUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Participants are able to understand the study protocol, requirements, and restri... [+4]

Contraindications to magnetic resonance imaging (MRI) or transcranial magnetic s... [+5]

Status: Recruiting

A Multicenter, Randomized, Crossover Clinical Trial Study of Digital Intelligence Software in Patients With MAFLD

Cirrhosis associated with metabolic associated fatty liver disease (MAFLD) can lead to a series of adverse outcomes in and outside the liver, but there is no approved treatment so far. In recent years, the prevalence of MAFLD-related cirrhosis in our country is increasing rapidly, but its clinical, pathological characteristics and natural prognosis are not clear, and there is a lack of standardized and effective prevention and treatment strategies.Through"Digital Intelligence software" to assist clinicians in MAFLD patients with remote data intervention, lifestyle intervention guidance and follow-up management, to evaluate the efficacy and safety of the intervention software on body weight and blood glucose in patients with MAFLD.

Participants needed: 2,000
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: The Affiliated Hospital of Hangzhou Normal UniversityUpdated: Nov 18, 2025Locations: 1
Eligibility criteria

Adult patients aged 18-65 years with a BMI of 24-35 kg/m². [+4]

Evidence of cirrhosis, defined as histological stage F4 or its clinical equivale... [+28]

Status: Not yet recruiting

Chinese Cardiologists' Knowledge/Practices on Flu Vaccine for Chronic Coronary Syndrome

This long-term single-center cross-sectional study evaluates physicians' knowledge of influenza vaccination in CCS patients through collected feedback, while identifying knowledge gaps and misconceptions regarding vaccination. By analyzing factors influencing physicians' recommendation practices, it provides evidence to guide future educational and policy interventions. Ultimately, the study aims to enhance cardiologists' vaccination awareness, thereby optimizing CCS patient management and reducing influenza-associated complications and mortality.

Participants needed: 5,000
Trial details
Biological sex: AllType: ObservationalSponsor: The Affiliated Hospital of Hangzhou Normal UniversityUpdated: Jun 4, 2025Locations: 1
Eligibility criteria

Physicians from non-cardiology specialties (e.g., surgery, general internal medi... [+1]

Status: Recruiting

Acute Effects of Meteorological Factors and Air Pollution on Cardiovascular Health

The goal of this observational study is to analyze the acute effects of meteorological factors and air pollution on cardiovascular system. The main question it aims to answer is: 1. How do meteorological factors and air pollution affect cardiovascular system? 2. What is the interaction between meteorological factors and air pollution on cardiovascular system? Participants will: 1. Provide their health data obtained in physical examination, including but not limited to blood pressure, blood routine, urine routine and B-ultrasound. 2. agree that the research team will use their personal identification number, gender, age, education level and other information for statistical analysis of the data.

Participants needed: 350,000
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: The Affiliated Hospital of Hangzhou Normal UniversityUpdated: Oct 29, 2024Locations: 1
Eligibility criteria

Relevant records in the physical examination database shall be ≥3times [+3]

Status: Not yet recruiting

Study on MAFLD-related Cirrhosis Prevention and Treatment Strategies

To establish a prospective, multicenter, biopsie-confirmed clinical cohort of MAFLD-related cirrhosis (F3-F4) in China, and analyze the clinical, histopathological features and natural outcomes of MAFLD-associated liver fibrosis/cirrhosis in China. And than to conducted a real-world study of different strategies of Chinese characteristics for the prevention and treatment of MAFLD-related cirrhosis to evaluate the efficacy and safety of the strategies.

Participants needed: 1,000
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: The Affiliated Hospital of Hangzhou Normal UniversityUpdated: Nov 18, 2023
Eligibility criteria

Age 18-75 years old, gender and ethnicity are not limited; [+3]

Cirrhosis due to any chronic liver disease other than MAFLD (including but not l... [+3]