Actively Recruiting
Construction of a Biobank for a Specialized Cohort of Portal Hypertension Observational Study Including Cirrhotic and Non-Cirrhotic Patients
Led by Shanghai Zhongshan Hospital · Updated on 2026-02-19
1000
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating portal hypertension and its serious complication, esophageal and gastric variceal bleeding (EGVB), which has high risks of bleeding, rebleeding, and death. This observational study focuses on expanding a biobank for portal hypertension by extending clinical cohort data over time and collecting diverse biological samples. The aim is to improve understanding of the disease, especially in patients with cirrhotic and non-cirrhotic portal hypertension, through multi-omics and advanced data analysis techniques. The study observes patients with portal hypertension who either have liver cirrhosis or do not. Participants receive endoscopic treatments such as ligation and cyanoacrylate injection, which are standard procedures used to manage variceal bleeding. The study collects clinical and imaging data, including abdominal CT scans, to support the biobank and provide detailed medical information for research. Participants will be followed for up to one year to monitor outcomes like rebleeding rates, death, and complications related to portal hypertension. The study involves collecting medical histories, imaging results, and treatment responses to provide comprehensive data for analysis. This long-term follow-up and data collection support developing improved clinical decision tools using artificial intelligence and multi-omics technologies.
CONDITIONS
Brief Title
Construction of a Portal Hypertension Biobank
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinically diagnosed with portal hypertension complicated by esophagogastric varices.
- Underwent abdominal CT examination.
- Age 18 years or older.
You will not qualify if you...
- Imaging or endoscopic evidence showing absence of esophageal and/or gastric varices.
- CT image quality not meeting study requirements.
- Incomplete medical history data.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 month
Participants undergo diagnostic assessments including abdominal CT examinations and endoscopic evaluation to confirm portal hypertension and presence of esophagogastric varices.
1 to 2 visits depending on assessments
Duration - 1 year
Participants are observed for clinical outcomes such as rebleeding, death, and complications over one year following diagnosis or treatment.
Periodic visits over 1 year as per routine care
Trial Site Locations
Total: 1 location
1
Zhongshan Hospital, Fudan University
Shanghai, Shanghai Municipality, China, 200000
Actively Recruiting
Research Team
X
Xiaoquan Huang, M.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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