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Diagnosis of Variceal Bleeding and Its Control in Cirrhosis

Not Applicable
Terminated
Conditions
Cirrhosis
Registration Number
NCT00188097
Lead Sponsor
University Hospital, Angers
Brief Summary

The aim of the study was to determine the independent predictors of variceal bleeding and control of bleeding in cirrhosis as no scientific assessment have been perfomed until now

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
400
Inclusion Criteria
  • Cirrhotic patients admitted for an acute complication of cirrhosis
  • admission ≤ 6 hours of inclusion
Exclusion Criteria
  • Child-Pugh score > 13
  • Digestive hemorrhage
  • Non cirrhotic portal hypertension

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
variceal bleeding
Secondary Outcome Measures
NameTimeMethod

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