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NCT Number: NCT07358663

Treatment Outcomes for Portal Hypertension Esophageal and Gastric Varices

This study is a single-center, prospective cohort study based on real-world data. Patients with portal hypertension and esophagogastric varices were enrolled and divided into an endoscopic treatment group and a non-endoscopic treatment group (including patients receiving medical therapy, interventional procedures, or surgical treatment) according to whether they underwent endoscopic intervention. Baseline data, serum metabolites, CT imaging and endoscopic images, liver biopsy pathology, and other multi-omics data were integrated for both groups. Patients were followed up to compare adverse events after variceal treatment, including rebleeding and its causes, hepatic encephalopathy, ascites, subsequent treatments (such as regular endoscopic therapy, NSSB, and TIPS), and survival outcomes. Clinical characteristics of portal hypertension attributed to different etiologies, including hepatitis B, autoimmune liver disease, schistosomiasis, hematological disorders, and chemotherapy-induced liver injury, were compared. The efficacy and safety of endoscopic and interventional treatments for esophagogastric varices were evaluated. Factors influencing rebleeding rates among different treatment groups were analyzed, and reasons for inclusion in different groups were discussed.

Recruiting

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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, China

Location status: Recruiting

Location contact

Xiaoquan Huang, M.D.

CONTACT

[email protected]

18801733835

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Clinical diagnosis of portal hypertension with esophagogastric varices.
  • Underwent abdominal CT and gastroscopy examinations.

Exclusion criteria

  • Presence of peptic ulcer, gastric tumor, or other causes of gastrointestinal bleeding confirmed by imaging or gastroscopy.
  • CT images of inadequate quality or incomplete medical history data.

Treatment and study plan

Primary outcomes

  1. Survival

    Time frame: At 1, 2, 6, and 12 months post-treatment

    Survival status

Secondary outcomes

  1. Adverse events

    Time frame: At 1, 2, 6, and 12 months post-treatment

    Post-treatment adverse events included rebleeding (and its causes), hepatic encephalopathy, and ascites

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

Assessment of Treatment Outcomes for Esophageal and Gastric Varices Secondary to Portal Hypertension

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jan 22, 2026
Registry last updated
May 14, 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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