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Improving Hepatitis C Treatment in Injection Drug Users

This study is ongoing, but not recruiting participants.
Study NCT00148031.   Last updated on July 10, 2008.   Information provided by National Institute on Drug Abuse (NIDA)

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Descriptive Information Fields
Brief Title  Improving Hepatitis C Treatment in Injection Drug Users
Official Title  Improving Hepatitis C Treatment in Injection Drug Users
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 improve the rate of HCV treatment completion and sustained virologic response (SVR) in IDUs will increase access by integrating HCV medical care into a substance abuse treatment program.

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 testing an intervention designed to improve the rate of HCV treatment completion and sustained virologic response (SVR) in IDUs. This intervention will increase access by integrating HCV medical care into a substance abuse treatment program. HCV infection is endemic among IDUs, and is associated with significant medical morbidity. While antiviral treatments are improving rapidly, providing HCV medical care for IDUs remains problematic for a number of reasons. IDUs often do not have adequate access to HCV diagnosis and treatment services, and they may have co-morbid psychiatric diagnoses that affect the ability to withstand the demands of HCV treatment. Therefore, this study will also examine psychiatric disorders and psychiatric symptoms in IDUs who are infected with Hepatitis C virus.

The proposed project is a five-year program consisting of a controlled clinical trial, studying 220 patients with HCV infection enrolled in methadone maintenance treatment (MMT). The HCV Medical Care Study is a randomized trial to test the efficacy of On-site HCV Medical Care provided at the MMT program versus Off-site care at the Gastroenterology (GI) Clinic. HCV antibody positive MMT patients (N=220) will be randomly assigned to receive HCV medical services either through an integrated delivery model located on-site in the MMT clinic, or through usual off-site referral to the GI Clinic. The main outcomes will be the rates of attaining SVR and completion of HCV treatment, as well as other measures of HCV-related health outcomes and quality of life. Participants will be evaluated for Axis I psychiatric diagnoses and will complete psychiatric measures at monthly intervals throughout the study. Psychiatric diagnosis will be made using the Structured Psychiatric Interview for the DSM-IV (SCID) and psychiatric symptom severity will be assessed for depression, mania, anxiety, and psychosis. Drug use measures, and quality of life measures will also be obtained. These data are expected to yield new knowledge about the efficacy of providing on-site HVC medical care in substance abuse treatment programs. They will provide a comparison of psychiatric diagnoses and psychiatric symptom presentation in HCV positive IDUs who choose to receive HCV treatment and those who do not choose to follow through with HCV treatment and will describe changes in psychiatric symptoms before, during, and after HCV medical care. Finally, the studies will also provide information about the influence of psychiatric symptoms and drug and alcohol use on HCV medical outcomes such as treatment completion and SVR.

Study Phase Phase IV
Study Type  Interventional
Study Design  Treatment, Randomized, Open Label, Parallel Assignment, Efficacy Study
Primary Outcome Measure  Efficacy of On-site versus Off-site delivery of HCV medical care for methadone maintenance treatment (MMT) patients, as evaluated by the proportion of patients achieving sustained virological response (SVR). [ Time Frame: 5 years ] [ Designated as safety issue: No ]
Secondary Outcome Measure  psychiatric diagnoses and symptom severity [ Time Frame: 5 years ] [ Designated as safety issue: No ]
Condition  Hepatitis C
Liver Diseases
Drug Abuse
Alcoholism
Intervention  Drug: Pegylated Interferon and Ribavirin
Behavioral: Psychosocial
Behavioral: On-site (MMT Clinic) HCV evaluation and treatment
Behavioral: Off-site HCV evaluation and treatment
MEDLINE PMIDs
Links State University of New York, Upstate Medical University This link exits the ClinicalTrials.gov site
Crouse Hospital, Chemical Dependency Treatment Services This link exits the ClinicalTrials.gov site
Recruitment Information Fields
Recruitment Status  Active, not recruiting
Enrollment  111
Start Date  September 2003
Completion Date November 2008
Eligibility Criteria 

Inclusion Criteria:

  1. 18-65 years of age.
  2. Enrolled in outpatient methadone maintenance treatment for greater than 3 months.
  3. Hepatitis C RNA positive.
  4. Willingness to accept HCV treatment.
  5. 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 Criteria:

  1. In need of inpatient drug or alcohol detoxification.
  2. Currently receiving the standard Hepatitis C treatment
  3. Unable to give adequate informed consent.
  4. Pregnant, nursing, or planning to become pregnant during HCV treatment or within 6 months following completion of treatment.
  5. 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.
  6. 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.
  7. 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.
  8. Subject did not attend all required screening appointments.
  9. Subject has a legal proceeding whose outcome may lead to incarceration within 3 months of intake.
Gender Both
Ages 18 Years to 65 Years
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00148031
Organization ID SUNY UMU IRB # 4929
Secondary IDs †† R01 DA016764
Study Sponsor  National Institute on Drug Abuse (NIDA)
Collaborators †† State University of New York - Upstate Medical University
Investigators 
Principal Investigator:     Steven L Batki, MD     State University of New York, Upstate Medical University - Department of Psychiatry    
Information Provided By National Institute on Drug Abuse (NIDA)
Verification Date July 2008
First Received Date  September 2, 2005
Last Updated Date July 10, 2008

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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