Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
400 participants
OBSERVATIONAL
2019-04-01
2023-10-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
OTHER
Study Groups
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EGD+NSBB
Patients receiving both endoscopic therapy and non-selective beta-blockers for treating high-risk esophagogastric varices
No interventions assigned to this group
EGD
Patients receiving mono endoscopic therapy for treating high-risk esophagogastric varices
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Adult patients aged 18-75 years;
3. Willing to anticipate and informed consent form obtained
Exclusion Criteria
2. Non-sinusoidal cirrhosis (e.g. vascular cirrhosis);
3. Coexistence with advanced hepatocellular carcinoma or other malignancies;
4. Coexistence with severe systemic diseases and less than 3 months of expected survival time;
5. Acute infection within 4 weeks before recruitment;
6. Antibiotic use within 4 weeks before recruitment;
7. Initial antiviral therapy for HBV or HCV within 4 weeks before recruitment;
8. Pregnant or lactating women;
9. Patients resistant to long-term follow-up
18 Years
75 Years
ALL
No
Sponsors
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National Natural Science Foundation of China
OTHER_GOV
Third Affiliated Hospital, Sun Yat-Sen University
OTHER
Responsible Party
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Jinlai Liu
Clinical Professor
Principal Investigators
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Bin Wu, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Department of Gastroenterology, Third Affiliated Hospital of Sun Yar-sen University
Locations
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Department of Cardiology, the Third Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China
Countries
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Other Identifiers
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SILC
Identifier Type: -
Identifier Source: org_study_id