Status:

COMPLETED

Improving Hepatitis C Treatment in Injection Drug Users

Lead Sponsor:

State University of New York - Upstate Medical University

Conditions:

Hepatitis C

Liver Diseases

Eligibility:

All Genders

18-65 years

Phase:

PHASE4

Brief Summary

The overall goal of the research project is to improve the outcome of medical care for injection drug users (IDUs) with Hepatitis C viral (HCV) infection. Hypothesis: An intervention designed to impr...

Detailed Description

The overall goal of the proposed health services research project is to improve the outcome of medical care for injection drug users (IDUs) with Hepatitis C viral (HCV) infection. This will be done by...

Eligibility Criteria

Inclusion

  • 18-65 years of age.
  • Enrolled in outpatient methadone maintenance treatment for greater than 3 months.
  • Hepatitis C RNA positive.
  • Willingness to accept HCV treatment.
  • Subject has non-VA (Veteran's Administration) medical insurance or is willing to bear any and all expenses associated with Hepatitis C medical treatment.

Exclusion

  • In need of inpatient drug or alcohol detoxification.
  • Currently receiving the standard Hepatitis C treatment
  • Unable to give adequate informed consent.
  • Pregnant, nursing, or planning to become pregnant during HCV treatment or within 6 months following completion of treatment.
  • Male subject who has a female sexual partner who is pregnant or planning to become pregnant at any time during HCV treatment or within 6 months following completion of treatment.
  • Female subject or male subject who has a female sexual partner who is of child bearing years and not using two medically approved forms of contraception.
  • Subject has made a commitment to attend residential care psychiatric or drug/alcohol rehabilitation, which would lead to unavailability to attend regularly scheduled medical care and research visits.
  • Subject did not attend all required screening appointments.
  • Subject has a legal proceeding whose outcome may lead to incarceration within 3 months of intake.

Key Trial Info

Start Date :

September 1 2003

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2007

Estimated Enrollment :

111 Patients enrolled

Trial Details

Trial ID

NCT00148031

Start Date

September 1 2003

End Date

March 1 2007

Last Update

April 24 2013

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Crouse Chemical Dependency Treatment Services

Syracuse, New York, United States, 13210

2

SUNY Upstate Medical University - Department of Gastroenterology

Syracuse, New York, United States, 13210