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Diagnosis of Variceal Bleeding and Its Control in Cirrhosis

Primary Purpose

Cirrhosis

Status
Terminated
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Diagnosis of variceal bleeding and dits control in cirrhosis
Sponsored by
University Hospital, Angers
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cirrhosis

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

    Outcomes

    Primary Outcome Measures

    variceal bleeding

    Secondary Outcome Measures

    Full Information

    First Posted
    September 12, 2005
    Last Updated
    January 18, 2006
    Sponsor
    University Hospital, Angers
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00188097
    Brief Title
    Diagnosis of Variceal Bleeding and Its Control in Cirrhosis
    Official Title
    Diagnosis of Variceal Bleeding and Its Control in Cirrhosis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2005
    Overall Recruitment Status
    Terminated
    Study Start Date
    November 1999 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    June 2002 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University Hospital, Angers

    4. Oversight

    5. Study Description

    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

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cirrhosis

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    400 (false)

    8. Arms, Groups, and Interventions

    Intervention Type
    Behavioral
    Intervention Name(s)
    Diagnosis of variceal bleeding and dits control in cirrhosis
    Primary Outcome Measure Information:
    Title
    variceal bleeding

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    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
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Paul Cales, PHD
    Organizational Affiliation
    UH Angers
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Diagnosis of Variceal Bleeding and Its Control in Cirrhosis

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