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Correlates and Consequences of Increased Immune Activation in Injection Drug Users

Correlates and Consequences of Increased Immune Activation in Injection Drug Users

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01831284
Enrollment
201
Registered
2013-04-15
Start date
2012-12-31
Completion date
2014-09-30
Last updated
2014-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intravenous Drug Usage

Brief summary

The goal of this study is to learn how injection drug use may affect the immune system.

Detailed description

The goal of this study is to learn how injection drug use may affect the immune system. One way to measure this is by looking at the blood and the gut, or gastrointestinal tract at the same time. It is thought that activating the immune system by injection drug use may increase destruction of immune cells in the gut. To test this theory, the investigators are enrolling HIV-negative injection drug users, HIV-negative people who do not use drugs and HIV-negative former injection drug users.

Interventions

PROCEDURESigmoidoscopy with biopsy

Sigmoidoscopy with biopsy

Sponsors

Rockefeller University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Ability to give informed consent * Between the ages of 18 and 55 * Absence of medical conditions that would preclude flexible sigmoidoscopy * Absence of active opportunistic infection requiring active therapy including antibiotics or anti-neoplastics (note this does not include prophylactic antibiotic therapy)

Exclusion criteria

* History of bleeding disorder * Platelet count below 70,000 * INR\>1.5 or PTT\>2X control * Active use of anticoagulants or aspirin therapy that cannot be interrupted * Comorbid diagnosis of inflammatory bowel disease * Pregnancy, incarceration, mentally disabled individuals * HIV-1 infection * Currently on Hepatitis C treatment

Design outcomes

Primary

MeasureTime frameDescription
Examine the behavioral and immunological correlates of increased immune activation in active and former injection drug users (IDUs) in blood and tissue.3 monthsDetailed assessments of blood and GI tissue including measurements of HCV viremia in 1) active HIV-1-uninfected IDUs (N=48) 2) a cohort of individuals entering or in drug treatment programs who have stopped injecting for approximately 1 and 3 months (N=48), the majority of whom we anticipate will be infected with HCV; and 3) non-injecting controls (N=48). In addition to obtaining blood and tissue, we will collect behavioral data including injection and other drug use and sexual behaviors.

Secondary

MeasureTime frameDescription
Determine the mechanisms of increased immune activation associated with active IDU using a systems biology approach.3 monthsThis study will isolate specific cell populations from the peripheral blood as well as the GALT that mediate innate and adaptive immune responses. We will perform transcriptional profiling with the goal of identifying gene expression patterns of a-priori defined biological pathways and functional categories that associate with phenotypes of interest. Finally to complement and clarify the results of our in vivo studies, we will examine the in vitro effects of adding morphine and methadone and withdrawing opiates on T cell subsets of interest using a systems biology approach.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026