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GUD Clinical and Virologic Response to Acyclovir in HIV Negative African Women — PK/GUD  

Genital Herpes Clinical Trial

Official title:
Prospective Study of Pharmacokinetics, Clinical and Virologic Response to Acyclovir Episodic Therapy for Genital Herpes Ulcers in HIV Negative African Women

Clinical Trial Summary

To examine the time to healing of genital lesion and duration of herpes simplex virus (HSV) shedding from genetic ulcer disease (GUD) among 90 HIV-negative African women who have a history of GUD and are HSV-2 seropositive and HIV-1 seronegative randomized in a 2:1 ratio to receive episodic acyclovir 400mg orally three times daily or matching placebo three times daily for 5 days and who are followed for a total of 13 days.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00808405
Study type Interventional
Source University of Washington
Contact
Status Completed
Phase N/A
Start date January 2009
Completion date July 2010
View Details
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