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Management of Hepatitis C in HIV-Infected and Uninfected IDUs
This study is currently recruiting participants.
Verified by National Institute on Drug Abuse (NIDA), July 2007
Sponsored by: National Institute on Drug Abuse (NIDA)
Information provided by: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier: NCT00496912
  Purpose

The purpose of this study is to determine if hepatitis C has damaged the liver, whether each subject's hepatitis C is treatable with currently available medicines, whether patient education groups before treatment help more patients start hepatitis C treatment, and if hepatitis C treatment with peginterferon and ribavirin given either by directly observed therapy or standard of care can be successfully given to persons who use or have used injection drugs.


Condition Intervention Phase
Hepatitis C Virus
HIV Infections
Drug: Peginterferon/Ribavirin
Phase IV

MedlinePlus related topics: AIDS Hepatitis Hepatitis C
Drug Information available for: Ribavirin
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Management of Hepatitis C in HIV-Infected and Uninfected IDUs

Further study details as provided by National Institute on Drug Abuse (NIDA):

Primary Outcome Measures:
  • 1. The proportion of IDUs who have clear medical contraindications to HCV treatment. 2. The prevalence of significant hepatic fibrosis among treatment eligible IDUs. 3. The proportion of treatment-eligible IDUs who initiate PEG/RBV therapy. [ Time Frame: 4 years ]

Secondary Outcome Measures:
  • The proportion of IDUs without clear contraindications who might be excluded by each of the 7 controversial contraindications. [ Time Frame: 4 years ]

Estimated Enrollment: 410
Study Start Date: January 2004
Estimated Study Completion Date: June 2008
Detailed Description:

Injection drug use is the predominant mode of hepatitis C (HCV) transmission in the United States and most injection drug users (IDUs) have HCV infection. HCV infection can cause progressive hepatic fibrosis (cirrhosis) over 20 or more years, leading, in some patients, to end-stage liver disease, hepatocellular carcinoma and death. Coinfection with human immunodeficiency virus (HIV) is present in 20-30% of HCV-infected IDUs, and is associated with the more rapid progression of HCV-related liver disease causing HCV infection to be considered as an opportunistic infection. While treatment of hepatitis C with pegylated interferon alfa and ribavirin (PEG/RBV) eradicates HCV infection in approximately one-half of patients, persons receiving methadone maintenance therapy, those who have recently used illicit drugs, and those with comorbidities (e.g., HIV infection, psychiatric disease) have been largely excluded from HCV treatment protocols. This research addresses the reality that the persons most affected by HCV infection (IDUs) are the least studied and the least treated, a disparity that becomes even more compelling as the success of HCV therapy increases. The principal goal of this research proposal is to expand the proportion of former and active injection drug users (IDUs) with HIV co-infection that benefit from hepatitis C care by assessing eligibility for treatment, medical necessity, and effectiveness of enhanced patient education prior to the initiation of HCV treatment among this patient population. To achieve these objectives, we plan to ask three fundamental questions: (1) what proportion of IDUs are eligible for hepatitis C virus (HCV) therapy based on both established and controversial criteria; (2) what proportion of IDUs currently need HCV treatment according to 2002 NIH consensus guidelines; and (3) what proportion of these treatment-eligible IDUs will initiate HCV therapy provided at no cost either as directly observed therapy compared to standard of care and is HCV treatment of IDUs more effective when enhanced patient education is provided prior to the initiation of HCV treatment. By answering these questions, we will 1) characterize the extent to which these various criteria affect treatment eligibility among IDUs; 2) define the magnitude of the medical need for treatment in these settings; and 3) evaluate the effectiveness of directly observed therapy versus standard of care and patient education on the initiation of HCV treatment. Overall, the study will provide much needed data to guide development of policies and guidelines for the treatment of HCV infection among IDUs, the largest risk group in the United States.

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Must use or have used injection drugs
  • Must have a reactive HCV antibody

Exclusion Criteria:

  • Does not have an absolute contraindication to HCV treatment:

    • HCV RNA not detected by PCR.
    • Pregnant or not willing to use birth control.
    • Life expectancy < 2 years.
    • Severe depression with suicidal ideation.
    • Allergic reaction to PEG/RBV.
    • Severe hematologic abnormality that is likely to be exacerbated by treatment.
    • Renal insufficiency.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00496912

Contacts
Contact: Beulah P Sabundayo, PharmD, MPH 443.287.6404 bsabund1@jhmi.edu
Contact: Yvonne Higgins, PA 410.614.0440 yhiggins@jhmi.edu

Locations
United States, Maryland
Johns Hopkins University Recruiting
Baltimore, Maryland, United States, 21287
Sub-Investigator: David L Thomas, MD, MPH            
Sub-Investigator: Stephanie Strathdee, PhD            
Sub-Investigator: Michael Torbenson, MD            
Sub-Investigator: Richard D Moore, MD, MHS            
Sub-Investigator: Greg Lucas, MD, PhD            
Sub-Investigator: Shruti Mehta, PhD            
Sub-Investigator: Sherilyn Brinkley, CRNP            
Sub-Investigator: Beulah P Sabundayo, PharmD, MPH            
Sponsors and Collaborators
Investigators
Principal Investigator: Mark S Sulkowski, MD Johns Hopkins University
  More Information

Publications of Results:
Other Publications:
Study ID Numbers: RO1 DA016065-01
Study First Received: July 5, 2007
Last Updated: July 9, 2007
ClinicalTrials.gov Identifier: NCT00496912  
Health Authority: United States: Institutional Review Board;   United States: Federal Government

Keywords provided by National Institute on Drug Abuse (NIDA):
Hepatitis C virus
HIV
IV Drug users
Treatment Naive
Treatment Experienced

Study placed in the following topic categories:
Sexually Transmitted Diseases, Viral
Liver Diseases
Acquired Immunodeficiency Syndrome
Ribavirin
Hepatitis, Viral, Human
Immunologic Deficiency Syndromes
Hepatitis
Virus Diseases
Digestive System Diseases
HIV Infections
Sexually Transmitted Diseases
Hepatitis C
Retroviridae Infections

Additional relevant MeSH terms:
RNA Virus Infections
Slow Virus Diseases
Flaviviridae Infections
Immune System Diseases
Lentivirus Infections
Infection

ClinicalTrials.gov processed this record on January 16, 2009