BACKGROUND: It is uncertain whether episodic acyclovir will enhance ulcer healing if delivered at primary health care settings, because there is often a delay in treatment initiation. METHODS: A double-blind, randomized, placebo-controlled trial of 5-day acyclovir (400 mg 3 times daily) was conducted among men with genital ulcers in South Africa. Participants received syndromic management; were tested for ulcer etiology, human immunodeficiency virus (HIV), syphilis, and herpes simplex virus type 2 (HSV-2); and were seen over the course of a month to evaluate ulcer healing and HIV-1 RNA shedding. Outcomes were ulcer duration and HIV-1 RNA shedding, assessed on day 7 among HIV-1-seropositive participants with a herpetic ulcer. RESULTS: A total of 309 men receivedacyclovir, and 306 received placebo; 63% were HIV-1 positive. There were 295 HIV-1-positive participants with a herpetic ulcer. Acyclovir improved ulcer healing--61% of those receiving acyclovir healed by day 7, compared with 42% of those receiving placebo (adjusted relative risk, 1.4 [95% confidence interval, 1.1-1.8]; P= .003). Acyclovir also improved healing by a median of 3 days (P= .002) and reduced HIV-1 ulcer shedding on day 7 (24% for acyclovir vs 37% for placebo; P= .05). CONCLUSIONS: Addition of acyclovir to syndromic management will improve healing of genital ulcers and may potentially reduce HIV transmission in combination with other interventions.
RCT Entities:
BACKGROUND: It is uncertain whether episodicacyclovir will enhance ulcer healing if delivered at primary health care settings, because there is often a delay in treatment initiation. METHODS: A double-blind, randomized, placebo-controlled trial of 5-day acyclovir (400 mg 3 times daily) was conducted among men with genital ulcers in South Africa. Participants received syndromic management; were tested for ulcer etiology, human immunodeficiency virus (HIV), syphilis, and herpes simplex virus type 2 (HSV-2); and were seen over the course of a month to evaluate ulcer healing and HIV-1 RNA shedding. Outcomes were ulcer duration and HIV-1 RNA shedding, assessed on day 7 among HIV-1-seropositiveparticipants with a herpetic ulcer. RESULTS: A total of 309 men received acyclovir, and 306 received placebo; 63% were HIV-1 positive. There were 295 HIV-1-positive participants with a herpetic ulcer. Acyclovir improved ulcer healing--61% of those receiving acyclovir healed by day 7, compared with 42% of those receiving placebo (adjusted relative risk, 1.4 [95% confidence interval, 1.1-1.8]; P= .003). Acyclovir also improved healing by a median of 3 days (P= .002) and reduced HIV-1 ulcer shedding on day 7 (24% for acyclovir vs 37% for placebo; P= .05). CONCLUSIONS: Addition of acyclovir to syndromic management will improve healing of genital ulcers and may potentially reduce HIV transmission in combination with other interventions.
Authors: Jared M Baeten; Stewart E Reid; Sinead Delany-Moretlwe; James P Hughes; Richard S Wang; Ellen Wilcox; Mohammed Limbada; Godspower Akpomiemie; Lawrence Corey; Anna Wald; Connie Celum Journal: Sex Transm Dis Date: 2012-01 Impact factor: 2.830
Authors: David Cal Ham; Susan Hariri; Mary Kamb; Jennifer Mark; Ricky Ilunga; Sara Forhan; Mupatal Likibi; David A Lewis Journal: Sex Transm Dis Date: 2016-01 Impact factor: 2.830
Authors: Deborah J Donnell; Jared M Baeten; Ting Hong; Jairam R Lingappa; Andrew Mujugira; Edith Nakku-Joloba; David Bangsberg; Connie Celum Journal: AIDS Behav Date: 2013-02
Authors: Anna M Foss; Peter T Vickerman; Philippe Mayaud; Helen A Weiss; B M Ramesh; Sushena Reza-Paul; Reynold Washington; James Blanchard; Stephen Moses; Catherine M Lowndes; Michel Alary; Charlotte H Watts Journal: Sex Transm Infect Date: 2010-11-08 Impact factor: 3.519