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NCT Number: NCT07419724

Construction of a Portal Hypertension Biobank

Esophageal and gastric variceal bleeding (EGVB) is a severe complication of portal hypertension (PH), characterized by high bleeding volume, high rebleeding rate, and high mortality. In recent years, endoscopic treatment has significantly improved therapeutic efficacy and patient survival. However, due to substantial individual variations among patients, individualized stratified management is crucial. For special populations with cirrhotic portal hypertension, clear management guidelines and clinical research evidence are lacking. The incidence of non-cirrhotic portal hypertension is increasing year by year; it has complex etiologies, lacks specific symptoms and imaging features, and poses diagnostic challenges. Currently, multi-omics research on portal hypertension is insufficient. The integration of multi-omics technologies, including genomics, radiomics, metabolomics, and gut microbiota, holds promise for a more comprehensive understanding of the pathogenesis. With continuous improvements in multi-modal medical data fusion technology, there is an urgent need to develop clinical decision support systems by combining standardized multi-omics databases with artificial intelligence techniques, thereby enhancing clinical decision-making capabilities and prognostic assessment.

This study aims to expand the established portal hypertension biobank by extending the temporal depth of clinical cohort data and diversifying sample types.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Zhongshan Hospital, Fudan University

Shanghai, Shanghai Municipality, 200000, China

Location status: Recruiting

Location contact

Xiaoquan Huang, M.D.

CONTACT

[email protected]

86-18801733835

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinically diagnosed with portal hypertension complicated by esophagogastric varices.
  • Underwent abdominal CT examination

Exclusion criteria

  • Imaging or endoscopic evidence demonstrating absence of esophageal and/or gastric varices.
  • CT image quality not meeting requirements or incomplete medical history data.

Treatment and study plan

Endoscopic treatment

Procedure

Endoscopic treatment including ligation and cyanoacrylate injection

Primary outcomes

  1. One-year rebleeding

    Time frame: Within 1 year

Secondary outcomes

  1. Death

    Time frame: Within 1 year

  2. Complications

    Time frame: Within 1 year

    Portal hypertension-related complications (including ascites, hepatic encephalopathy, portal vein thrombosis, etc.)

Study contacts

Contact information is provided by the study sponsor or research team.

Xiaoquan Huang, M.D.

CONTACT

[email protected]

86-18801733835

Sponsors and collaborators

Lead sponsor

Shanghai Zhongshan Hospital

Other

Registry information

Official study title

Construction of a Biobank for a Specialized Cohort of Portal Hypertension

Important dates

Study start
2025
Primary completion
2028
Study completion
2031
First posted
Feb 19, 2026
Registry last updated
Feb 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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