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Sponsored by: |
National Institute on Drug Abuse (NIDA) |
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Information provided by: | National Institute on Drug Abuse (NIDA) |
ClinicalTrials.gov Identifier: | NCT00496912 |
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 |
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Hepatitis C Virus HIV Infections |
Drug: Peginterferon/Ribavirin |
Phase IV |
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 |
Estimated Enrollment: | 410 |
Study Start Date: | January 2004 |
Estimated Study Completion Date: | June 2008 |
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.
Ages Eligible for Study: | 18 Years to 70 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Does not have an absolute contraindication to HCV treatment:
Contact: Beulah P Sabundayo, PharmD, MPH | 443.287.6404 | bsabund1@jhmi.edu |
Contact: Yvonne Higgins, PA | 410.614.0440 | yhiggins@jhmi.edu |
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 |
Principal Investigator: | Mark S Sulkowski, MD | Johns Hopkins University |
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 |
Hepatitis C virus HIV IV Drug users Treatment Naive Treatment Experienced |
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 |
RNA Virus Infections Slow Virus Diseases Flaviviridae Infections |
Immune System Diseases Lentivirus Infections Infection |