Pharmacokinetics and dose proportionality of three Tramadol Contramid OAD tablet strengths

Biopharm Drug Dispos. 2007 Sep;28(6):323-30. doi: 10.1002/bdd.561.

Abstract

A three-way crossover study in 27 human volunteers was conducted to characterize the pharmacokinetics and to assess the dose proportionality of 100 mg, 200 mg and 300 mg strengths of a novel once-a-day tramadol controlled-release tablet (Tramadol Contramid OAD) following single-dose administration. Serial blood samples were collected at predefined timepoints over a 48 h period and racemic tramadol and O-desmethyltramadol concentrations in plasma were determined using a validated LC-MS/MS method. Pharmacokinetic parameters were derived using noncompartmental methods. Following dose normalization and logarithmic transformation of concentration-dependent parameters, the results were compared using analysis of variance (ANOVA). The residual variability thereby obtained was used to construct 90% classical confidence intervals. The two one-sided tests procedure was used for all pairwise comparisons. Dose proportionality was concluded since the 90% CI for the ratio of geometric means was included in the acceptance range of 0.80-1.25 for all comparisons.

Publication types

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

MeSH terms

  • Adult
  • Analgesics, Opioid / adverse effects
  • Analgesics, Opioid / metabolism
  • Analgesics, Opioid / pharmacokinetics*
  • Area Under Curve
  • Aspartate Aminotransferases / blood
  • Chromatography, High Pressure Liquid
  • Cross-Over Studies
  • Dizziness / chemically induced
  • Dose-Response Relationship, Drug
  • Half-Life
  • Humans
  • Male
  • Nausea / chemically induced
  • Pruritus / chemically induced
  • Tablets, Enteric-Coated
  • Tandem Mass Spectrometry
  • Tramadol / blood
  • Tramadol / metabolism
  • Tramadol / pharmacokinetics*
  • Vomiting / chemically induced

Substances

  • Analgesics, Opioid
  • Tablets, Enteric-Coated
  • Tramadol
  • Aspartate Aminotransferases