Directly Administered Antiretroviral Therapy (DAART) Among HIV-1infected Injecting Drug Users (IDUs) in Chennai, India (DAART+)

This study has been withdrawn prior to enrollment.
(No participants satisfied eligibility criteria and were enrolled into the study since July 2008.)
Sponsor:
Collaborator:
Information provided by:
Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT00709007
First received: July 1, 2008
Last updated: March 12, 2009
Last verified: March 2009

July 1, 2008
March 12, 2009
July 2008
July 2010   (final data collection date for primary outcome measure)
HIV RNA < 400 copies/ml [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00709007 on ClinicalTrials.gov Archive Site
  • Incidence of mortality and/or AIDS-defining illnesses [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
  • Change in absolute CD4+ count from baseline [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
  • Incidence of antiretroviral drug resistance [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Directly Administered Antiretroviral Therapy (DAART) Among HIV-1infected Injecting Drug Users (IDUs) in Chennai, India
Evaluating the Role of Directly Administered Antiretroviral Therapy (DAART) in Conjunction With Opiate Substitution in Delivery of Highly Active Antiretroviral Therapy to HIV-1-Infected Injecting Drug Users (IDUs) in Chennai, India

Though the HIV epidemic in India is predominantly among heterosexual populations, it is estimated that there are approximately 1.1 million injection drug users (IDUs) in India with HIV prevalence as high as 64% among IDUs in certain cities. In April 2004, the government of India launched a free-antiretroviral therapy roll-out program aimed at initiating 100,000 persons on HAART. Similar guidelines are currently being followed for the delivery and choice of HAART for IDU and non-IDU populations. However, IDUs have certain issues that complicate the delivery of HAART that need to be addressed by delivery programs such as delayed access to care, poor perceived adherence, and more rapid disease progression. This proposal will assess the feasibility and effectiveness of directly administered antiretroviral therapy (DAART) in conjunction with opioid substitution as a mode of delivery of HAART to IDUs in Chennai, India. To evaluate this objective we will conduct a randomized controlled pilot study of DAART vs self-administered therapy (SAT) among 100 HIV-1 infected treatment naïve IDUs who are enrolled in an opioid substitution program in Chennai and compare the following outcomes between the two arms: Primary Endpoint: Proportion of participants with viral load (VL) <400 copies/ml at 24 and 48 weeks; Secondary Endpoints: (1) Incidence of mortality and AIDS-defining illnesses at 24 and 48 weeks, (2) Changes in absolute CD4+ count from baseline at 24 and 48 weeks, and (3) Incidence of antiretroviral drug resistance at 24 and 48 weeks. Intention-to-treat analyses will be used. The study objective is in line with the priority areas identified in the Indian National AIDS Control Program Phase III (NACP III) and the results of this study will help inform the government of India on appropriate modes of delivery of HAART to IDUs. This study will also be among the first studies to be conducted in India to evaluate two different modes of delivery of HAART to IDUs.

Not Provided
Interventional
Phase 2
Phase 3
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • HIV Infections
  • Heroin Dependence
  • Behavioral: Directly Administered Antiretroviral Therapy (DAART)
    Participants are observed taking HIV medications by study staff on days when they receive opioid agonist therapy (sub-lingual buprenorphine) at the clinic.
  • Behavioral: SAT
    Participants take their HIV medications by themselves.
  • Experimental: DAART
    Participants are observed taking HIV medications by study staff on days when they receive opioid agonist therapy (sub-lingual buprenorphine) at the clinic.
    Intervention: Behavioral: Directly Administered Antiretroviral Therapy (DAART)
  • Active Comparator: SAT
    Participants take their HIV medications on their own but visit the clinic for opioid agonist substitution therapy.
    Intervention: Behavioral: SAT
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
100
July 2011
July 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. 18 years of age or older
  2. Provide written informed consent
  3. Permanent residence should be less than or equal to 15 kms (9.5 miles) from the YRGCSAR clinic
  4. Be an injection drug user (by self-report)
  5. Satisfy criteria for opioid dependence as per the DSM-IV criteria (see Appendix)
  6. Urine screening must test positive for presence of opioids
  7. Documented evidence of HIV infection (double ELISA: Murex HIV-1.2.O, Abbott Murex, UK and Vironostika® HIV Uni-form II Ag/Ab, Biomérieux, The Netherlands)
  8. Be ART naïve (by self-report)
  9. If female of childbearing potential (all of the following)

    • Have a negative urine pregnancy test
    • Be willing to use barrier based or oral contraceptive for the duration of the study if sexually active.
  10. Satisfy Indian National Guidelines for initiation of HAART (any of the following)

    • Absolute CD4+ count < 200 cells/ µl
    • AIDS-defining illness with any CD4+ count
    • Absolute CD4+ count between 200 - 350 cell/ µl with HIV-related symptoms

Exclusion Criteria:

  1. Requires a liquid preparation of ART or ART needs to be dosed more than twice daily
  2. Indicates an intention to migrate in the next 48 weeks
  3. Clinical or radiological signs of active tuberculosis
  4. Any medical or psychiatric condition that the study physician believes to be a contraindication to study participation.
  5. Enrolled in another HIV treatment program
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
India
 
NCT00709007
R01-DA018577-03S1
No
Gregory M Lucas, Johns Hopkins University School of Medicine
Johns Hopkins University
National Institute on Drug Abuse (NIDA)
Principal Investigator: Gregory M Lucas, MD,PhD Johns Hopkins University School of Medicine, USA
Johns Hopkins University
March 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP