CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 440 enrolled
Drug / intervention
Acyclovir +1 moredrug
Likely dose
Acyclovir 400mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00405821
NCT00405821Phase 2Completed

A Randomized, Double-Blind, Placebo-Controlled Trial of Acyclovir Prophylaxis Versus Placebo Among HIV-1/HSV-2 Co-Infected Individuals in Uganda

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Nov 30, 2006·Updated Sep 28, 2012

In Brief

A Phase 2 clinical trial evaluating Acyclovir and Placebo for HIV Infections and Herpes Genitalis. Completed, enrolled 440 participants across 1 site.

Detailed Summary

This study will determine whether acyclovir, a medicine used to treat herpes simplex virus 2 (HSV-2), can slow down the progression (worsening) of HIV disease in people with both HIV and HSV-2 infections. HSV-2 increases the amount of HIV virus in the blood of infected people and may make HIV progress faster. The study will evaluate: "Whether people who take acyclovir can avoid antiretroviral treatment until later in their lives "Whether people who take acyclovir get fewer genital ulcers "How well people are able to take acyclovir and any side effects they experience from it "Differences in the amount of HIV virus in the blood of patients who are and are not taking acyclovir, and how HIV/AIDS is different in these patients. People 18 years of age and older living in the Rakai district of Uganda who are infected with both HIV (early stage disease) and HSV-2 may be eligible for this study. Participants are randomly assigned to take the study drug, acyclovir, or a placebo (look-alike pill with no active ingredient) daily for 2 years. During this time, they visit the clinic once a month for a routine physical examination. Patients who develop genital ulcers or complications of HIV are treated for the problem, and patients whose HIV disease progresses, requiring them to begin antiretroviral therapy, are treated accordingly.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUganda

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 30, 2006
Enrollment StartNov 1, 2006
Primary CompletionOct 1, 2010
Study CompletionNov 1, 2010
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 19.6 years ago

Interventions

Acyclovirdrug

400mg twice daily for 24 months

Placebodrug

Placebo tablet twice daily for 24 months