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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00188097
Date of registration: 12/09/2005
Primary sponsor: University Hospital, Angers
Public title: Diagnosis of Variceal Bleeding and Its Control in Cirrhosis
Scientific title: Diagnosis of Variceal Bleeding and Its Control in Cirrhosis
Date of first enrolment: November 1999
Target sample size: 400
Recruitment status: Terminated
URL:  http://clinicaltrials.gov/show/NCT00188097
Study type:  Interventional
Study design:  Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention  
Countries of recruitment
Contacts
Name:   Paul Cales, PHD
Address: 
Telephone:
Email:
Affiliation:  UH Angers
Key inclusion & exclusion 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



Age minimum: 18 Years
Age maximum: 75 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Cirrhosis
Intervention(s)
Behavioral: Diagnosis of variceal bleeding and dits control in cirrhosis
Primary Outcome(s)
variceal bleeding
Secondary Outcome(s)
Secondary ID(s)
PHRC 03-04
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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