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A randomized, double-blind clinical trial of vaginal acidification versus placebo for the treatment of symptomatic bacterial vaginosis.

AbstractBACKGROUND AND OBJECTIVES:
Vaginal acidification has been suggested as a means of normalizing the vaginal flora.
GOAL:
The purpose of this study was to determine the effectiveness of an acetic acid-based vaginal gel in the treatment of bacterial vaginosis (BV).
STUDY DESIGN:
Forty-four patients with BV were enrolled in a randomized, double-blind clinic trial. Of these, 29 were evaluable. Patients were randomized to receive either 5 mL acetic acid gel (n = 14) or placebo gel (n = 15) intravaginally twice daily for 7 days. Clinical criteria and vaginal Gram stain scores were compared between the initial visit and at 2 weeks after initiating therapy.
RESULTS:
No significant differences were noted when comparing drug and placebo in terms of subjective or clinical improvement or improvement in Gram stain smears for bacterial vaginosis.
CONCLUSION:
Vaginal acidification with an acetic acid gel formulated to pH 3.9 to 4.1 was ineffective therapy for bacterial vaginosis.
AuthorsRobert L Holley, Holly E Richter, R Edward Varner, Lisa Pair, Jane R Schwebke
JournalSexually transmitted diseases (Sex Transm Dis) Vol. 31 Issue 4 Pg. 236-8 (Apr 2004) ISSN: 0148-5717 [Print] United States
PMID15028938 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Anti-Infective Agents
  • Vaginal Creams, Foams, and Jellies
  • Acetic Acid
Topics
  • Acetic Acid (administration & dosage, therapeutic use)
  • Administration, Intravaginal
  • Adult
  • Anti-Infective Agents (administration & dosage, therapeutic use)
  • Double-Blind Method
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Treatment Outcome
  • Vaginal Creams, Foams, and Jellies (administration & dosage, therapeutic use)
  • Vaginosis, Bacterial (drug therapy)

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