Comparison of 0.8% and 1.6% terconazole cream in severe vulvovaginal candidiasis

Obstet Gynecol. 1990 Sep;76(3 Pt 1):414-6.

Abstract

Terconazole is the first topical triazole antifungal agent. The results of several European clinical trials have shown both terconazole cream and suppositories to be effective and safe in the treatment of vulvovaginal candidiasis. We conducted a comparative placebo-controlled, double-blind study of 0.8 and 1.6% terconazole creams in a group of patients with persistent vulvovaginal candidiasis. In short-term evaluations (1-3 days and 8-11 days after therapy), 75% of patients receiving 0.8% terconazole cream were asymptomatic and 83.3% were mycologically cured. By 30-35 days after therapy, 75% were still asymptomatic and 58.3% were mycologically negative. No significant difference was seen between the results obtained with 0.8 and 1.6% terconazole creams. Safety data collected on these patients demonstrated that the side effects were rare and mild. This study confirms the efficacy and safety of topical terconazole in patients with vulvovaginal candidiasis.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Administration, Intravaginal
  • Adult
  • Antifungal Agents / administration & dosage
  • Antifungal Agents / therapeutic use*
  • Candidiasis, Vulvovaginal / drug therapy*
  • Chemistry, Pharmaceutical
  • Double-Blind Method
  • Female
  • Humans
  • Middle Aged
  • Random Allocation
  • Triazoles / administration & dosage
  • Triazoles / therapeutic use*
  • Vaginal Creams, Foams, and Jellies

Substances

  • Antifungal Agents
  • Triazoles
  • Vaginal Creams, Foams, and Jellies
  • terconazole