Treatment Outcomes for Portal Hypertension Esophageal and Gastric Varices

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai Zhongshan Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Clinical diagnosis of portal hypertension with esophagogastric varices.

Underwent abdominal CT and gastroscopy examinations.

Disqualifiers

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.

Trial population

Patients admitted with portal hypertension and esophagogastric varices between January 2026 and December 2027 were included. Portal hypertension was defined as elevated portal pressure caused by various etiologies, including chronic viral hepatitis, metabolic-associated fatty liver disease, autoimmune liver disease, chemotherapy-induced liver injury, and hematological disorders. The diagnosis of portal hypertension and esophagogastric varices was confirmed by laboratory tests and imaging studies.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,384 Participants
are grouped into 2 trial groups
Group A: Endoscopic treatment group
Group B: Non-endoscopic treatment group

Trial outcomes

Primary outcomes

1

Survival

Survival status

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

Secondary outcomes

1

Adverse events

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

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

Other outcomes

Sponsors and contacts

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