[Efficacy of a theophylline retard preparation administered at 3 different intake times additionally to basic medication]

Pneumologie. 1991 Nov:45 Suppl 4:842-7.
[Article in German]

Abstract

In this randomised crossover study in 26 outpatients with bronchial asthma the efficacy of a new once-daily theophylline formulation given in addition to a baseline medication was investigated; moreover, under steady state conditions, the effect of three evening intake times (6, 8 and 10 p.m.) on 24-hour pharmacokinetics and peak-expiratory flow profiles was evaluated. The theophylline dose had been individually titrated. The pharmacodynamic results show a marked improvement in 24-hour lung function data after adding theophylline to a drug therapy including inhalative anti-cholinergics in 50% of the treated outpatients. No significant differences between the pharmacokinetic characteristics and the 24-hour averages (mesors) of peak expiratory flow at the three different intake times 6, 8 and 10 p.m. were found; however, intake at 10 p.m. resulted in the highest nocturnal excess of serum theophylline concentrations and the highest peak expiratory flow during the early morning hours between 2 and 6 a.m.

Publication types

  • Clinical Trial
  • English Abstract
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Asthma / drug therapy*
  • Asthma / physiopathology
  • Circadian Rhythm
  • Female
  • Humans
  • Male
  • Middle Aged
  • Parasympatholytics / therapeutic use
  • Peak Expiratory Flow Rate / drug effects
  • Theophylline / administration & dosage*
  • Time Factors

Substances

  • Parasympatholytics
  • Theophylline