Oral acyclovir and herpes labialis: a randomized, double-blind, placebo-controlled study

J Am Dent Assoc. 1987 Jul;115(1):38-42. doi: 10.14219/jada.archive.1987.0211.

Abstract

A study of the effects of oral acyclovir (200 mg), administered five times per day for 5 days in 210 patients who cultured positive for herpes labialis, is made. A total of 149 patients were followed through three episodes each of herpes labialis while taking a placebo or acyclovir. Patients were evaluated for several clinical parameters, including the loss of lesion crust and reduction of the size of the area of the lesion between day 1 and day 5. Acyclovir showed a significant antiviral effect. Results show that oral acyclovir can favorably affect some parameters, but that higher doses or a "loading dose" could improve its efficacy.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyclovir / administration & dosage*
  • Administration, Oral
  • Adult
  • Clinical Trials as Topic
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Herpes Labialis / drug therapy*
  • Humans
  • Male
  • Middle Aged
  • Patient Compliance
  • Random Allocation

Substances

  • Acyclovir