drugset / Trial / NCT00257452

A Double-blind, Randomised Study to Assess the Influence of Tiotropium (Spiriva®)

NCT00257452

Phase 1 Completed 56 enrolled Boehringer Ingelheim
RandomizedCrossoverDouble-blindTreatment

Summary

To demonstrate that tiotropium (Spiriva®) does not prolong the QT interval of the ECG more than placebo

Timeline

Start
2004-10
Primary completion
2005-07
Completion
2005-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Moxifloxacin Small molecule 200 mg
Subject Tiotropium Other / unclassified 18 ug Inhaled
Subject Tiotropium Other / unclassified 54 ug Inhaled

Indications

No indication recorded.