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Effect of Large Volume Paracentesis on Fatigue in Cirrhosis

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status

Withdrawn

Conditions

Cirrhosis
Fatigue
Ascites

Study type

Observational

Funder types

Other

Identifiers

NCT00603200
0701008974

Details and patient eligibility

About

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).

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

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

Trial design

0 participants in 1 patient group

Group 1
Description:
Patients with cirrhosis, who have refractory ascites requiring large volume paracentesis

Trial contacts and locations

1

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Central trial contact

Samual Sigal, MD; Reem Sharaiha, MD

Data sourced from clinicaltrials.gov

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