CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 12 target
Drug / intervention
Rifampicin +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00985270
NCT00985270Phase 4Completed

PXR-agonisti Rifampisiinin Vaikutukset Glukoosi-, Lipidi- ja Hormonihomeostaasiin

University of Oulu·interventional·Posted Sep 28, 2009·Updated Feb 10, 2011

In Brief

A Phase 4 clinical trial evaluating Rifampicin and Placebo for Glucose Tolerance. Completed, enrolled 12 participants across 1 site.

Detailed Summary

This clinical trial is designed to study the effects of rifampicin on the glucose, lipid and hormone homeostasis in healthy volunteers. The main hypothesis is that rifampicin lowers fasting glucose and enhances insulin sensitivity. The study is a randomized, placebo-controlled, open-label cross-over trial. Twelve subjects will be given 600 mg of rifampicin a day for a week compared to a one-week placebo arm. There is at least a 4-week wash-out between the arms. The main outcome measures are the changes in the fasting glucose and HOMA-IR-index (calculated based on fasting glucose and insulin).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFinland
Collaborators--

Timeline

Phase 4CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedSep 28, 2009
Enrollment StartSep 1, 2009
Primary CompletionOct 1, 2010
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 16.8 years ago

Interventions

Rifampicindrug

Placebodrug