drugset / Trial / NCT00723229

A Randomized Trial to Evaluated the Suppressive Effect of Acyclovir on Rapidly Cleared HSV-2 Reactivation

NCT00723229

RandomizedCrossoverOpen-labelTreatment

Summary

We propose to study the episode rate, duration, and quantity of HSV-2 genital shedding in patients taking standard, FDA approved, CDC recommended doses of acyclovir (400 mg PO BID) for HSV-2 suppression compared to taking no medication to better define the effect of acyclovir on short bursts of rapidly cleared HSV-2 shedding. This study will be a randomized, open label, cross-over trial. We hypothesize that short bursts of HSV-2 reactivation will not be suppressed by acyclovir.

Timeline

Start
2008-08
Primary completion
2010-07
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acyclovir Small molecule 400 mg Oral