NCT00188097

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

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 1999

Typical duration for not_applicable

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 1999

Completed
2.6 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2002

Completed
3.3 years until next milestone

First Submitted

Initial submission to the registry

September 12, 2005

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 16, 2005

Completed
Last Updated

January 19, 2006

Status Verified

August 1, 2005

First QC Date

September 12, 2005

Last Update Submit

January 18, 2006

Conditions

Cirrhosis

Outcome Measures

Primary Outcomes (1)

  • variceal bleeding

Interventions

Diagnosis of variceal bleeding and dits control in cirrhosisBEHAVIORAL

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Cirrhotic patients admitted for an acute complication of cirrhosis

You may not qualify if:

  • Child-Pugh score \> 13
  • Digestive hemorrhage
  • Non cirrhotic portal hypertension

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Fibrosis

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Paul Cales, PHD

    UH Angers

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

September 12, 2005

First Posted

September 16, 2005

Study Start

November 1, 1999

Study Completion

June 1, 2002

Last Updated

January 19, 2006

Record last verified: 2005-08