Results of double-blind, multicentre study with ritodrine in premature labour

Br Med J. 1971 Jul 17;3(5767):144-7. doi: 10.1136/bmj.3.5767.144.

Abstract

A double-blind placebo-controlled multicentre study with ritodrine, a beta-mimetic uterine relaxant, has been performed in 91 patients in premature labour. All patients were treated according to a fixed dosage scheme consisting of an intravenous infusion followed by oral tablets for a total of seven days. Ritodrine arrested premature labour in 80%, the placebo in 48% of the patients (P=0.02). This short treatment, however, was usually not sufficient to prolong gestation till term. Apart from a slight to moderate rise in maternal heart rate and a slight rise in systolic blood pressure, ritodrine did not give rise to any maternal or fetal side effects. The problems of patient selection and of evaluation of the results are discussed.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adrenergic beta-Agonists / administration & dosage
  • Adrenergic beta-Agonists / adverse effects
  • Adrenergic beta-Agonists / therapeutic use
  • Adult
  • Amino Alcohols / administration & dosage
  • Amino Alcohols / therapeutic use*
  • Apgar Score
  • Blood Pressure / drug effects
  • Chemical Phenomena
  • Chemistry
  • Clinical Trials as Topic
  • Female
  • Gestational Age
  • Heart Rate / drug effects
  • Humans
  • Injections, Intravenous
  • Muscle Relaxants, Central / therapeutic use*
  • Obstetric Labor, Premature / prevention & control*
  • Phenethylamines / administration & dosage
  • Phenethylamines / therapeutic use*
  • Phenols / administration & dosage
  • Phenols / therapeutic use
  • Placebos
  • Pregnancy
  • Sympathomimetics / therapeutic use*
  • Uterus / drug effects

Substances

  • Adrenergic beta-Agonists
  • Amino Alcohols
  • Muscle Relaxants, Central
  • Phenethylamines
  • Phenols
  • Placebos
  • Sympathomimetics