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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00058903
Other study ID # TRCPWS (completed)
Secondary ID
Status Completed
Phase Phase 2
First received April 14, 2003
Last updated January 12, 2010
Start date April 2003
Est. completion date March 2005

Study information

Verified date January 2010
Source National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The goal of this study is to find an effective and well-tolerated medical therapy for itching due to liver disease. Persons with primary biliary cirrhosis or chronic hepatitis C are currently being enrolled in the study. Persons participating in the study are given sertraline, a medication which is also often used for depression,to treat their itching. The dose is gradually increased as the effect on itching and any other potential side effects are carefully monitored.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date March 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 21 Years to 80 Years
Eligibility - Itching for at least 3 months

- Primary biliary cirrhosis or hepatitis C

- Elevated alkaline phosphatase for at least 6 months

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
sertraline


Locations

Country Name City State
United States University of Texas Southwestern Medical Center at Dallas Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

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