The safety and efficacy of topical norfloxacin compared with placebo in the treatment of acute, bacterial conjunctivitis. The Norfloxacin-Placebo Ocular Study Group

Eur J Ophthalmol. 1992 Apr-Jun;2(2):58-66. doi: 10.1177/112067219200200202.

Abstract

Two hundred and eighty-four patients with acute conjunctivitis were enrolled in a double-masked study comparing norfloxacin ophthalmic solution with placebo. The proportion of patients who were clinically improved after 5 days treatment was 88.1% in the norfloxacin group and 71.6% in the placebo group (p less than 0.01). The proportion of patients who had all organisms eradicated, including the coagulase-negative staphylococci, after two to three days treatment was 52.7% for norfloxacin and 23.9% for placebo (p less than 0.01) and 64.7% and 26.3% (p less than 0.01) respectively when the coagulase-negative staphylococci were not included. Adverse experiences occurred in 4.2% of the patients receiving norfloxacin compared to 7.1% of the placebo patients. None of the adverse experiences was serious.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Acute Disease
  • Adult
  • Colony Count, Microbial
  • Conjunctivitis, Bacterial / drug therapy*
  • Conjunctivitis, Bacterial / microbiology
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Norfloxacin / administration & dosage
  • Norfloxacin / adverse effects
  • Norfloxacin / therapeutic use*
  • Ophthalmic Solutions
  • Placebos
  • Treatment Outcome

Substances

  • Ophthalmic Solutions
  • Placebos
  • Norfloxacin