Design, methods, and conduct of the Optic Neuritis Treatment Trial

Control Clin Trials. 1993 Apr;14(2):123-42. doi: 10.1016/0197-2456(93)90015-6.

Abstract

The Optic Neuritis Treatment Trial (ONTT) was an investigator-initiated, multi-centered, randomized, controlled clinical trial supported by cooperative agreements and grants. It was designed to evaluate the efficacy and safety of oral prednisone or intravenous methylprednisolone followed by oral prednisone as compared with oral placebo. The primary outcome measures were contrast sensitivity and visual field; secondary measures were visual acuity and color vision. Four hundred fifty-seven patients were followed for a minimum of 6 months and a maximum of 3 years. This article describes the design and the methods used to implement the ONTT.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Female
  • Humans
  • Male
  • Methylprednisolone / administration & dosage
  • Methylprednisolone / therapeutic use
  • Middle Aged
  • Optic Nerve / physiopathology*
  • Optic Neuritis / complications
  • Optic Neuritis / drug therapy
  • Optic Neuritis / physiopathology*
  • Placebos / administration & dosage
  • Placebos / therapeutic use
  • Prednisone / administration & dosage
  • Prednisone / therapeutic use
  • Treatment Outcome
  • Vision Disorders / complications
  • Vision Disorders / drug therapy
  • Vision Disorders / physiopathology

Substances

  • Placebos
  • Prednisone
  • Methylprednisolone