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NCT00603200 Clinical Trial

Effect of Large Volume Paracentesis on Fatigue in Cirrhosis

Fatigue Clinical Trial

Official title:
The Effect of Large Volume Paracentesis on Fatigue in Cirrhosis

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00603200
Other study ID # 0701008974
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 2008
Est. completion date December 2009

Study information
Verified date December 2023
Source Weill Medical College of Cornell University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purposeof this study is to determine the effect of a large volume paracentesis (procedure in whihc a catheter is placed to remove fluid from the abdomen) on the severity of fatigue i patients with cirrhosis (severe scarring of the liver) and large volume ascites (fluid in the abdomen).

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date December 2009
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - ambulatory patient with cirrhosis - baseline Cr <2 - ability to complete psychometric testing - refractory ascites Exclusion Criteria: - Cr >2 - history of Gastrointestinal bleed - history of infection - history of renal failure

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States New York Presbyterial, Weill Cornell medical College New York New York

Sponsors (1)
Lead Sponsor Collaborator
Weill Medical College of Cornell University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Improvement in Fatigue symptomatology, as defined by fatigue questionnairre instantly
Secondary Improvement in sleep post paracentesis
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