drugset / Trial / NCT01161472

A Study to Assess the Cognitive Effects of Fesoterodine in Elderly Subjects

NCT01161472 ↗

Phase 1 Completed 20 enrolled Pfizer
RandomizedCrossoverQuadruple-blind

Summary

The study is designed to evaluate elements of cognitive function in subjects receiving either fesoterodine or alprazolam.

Timeline

Start
2010-07
Primary completion
2010-09
Completion
2010-09

Outcome

Missed primary endpoint

registry Fesoterodine 4 mg vs Placebo; p = 0.1198; Least square (LS) Mean Difference -0.0285 (95% CI -0.0647 to 0.0077); ANCOVA NCT01161472 ↗

registry Fesoterodine 8 mg vs Placebo; p = 0.2459; LS Mean Difference -0.0203 (95% CI -0.0551 to 0.0145); ANCOVA NCT01161472 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Alprazolam Small molecule 1 mg —
Subject Fesoterodine Other / unclassified 4 mg —
Subject Fesoterodine Other / unclassified 8 mg —

Indications

No indication recorded.