Phase 2CompletedHealthspan endpoint

A Study of Fesoterodine and Oxybutynin on Cognitive Function in Mild Cognitive Impairment

A Double Blind, Randomized Four Way Cross Over Study to Compare the Effect of Fesoterodine 4mg and 8mg Once Daily and Oxybutynin 5mg Twice Daily After Steady State Dosing Versus Placebo on Cognitive Function in Subjects With Overactive Bladder, Over the Age of 75 Years With Mild Cognitive Impairment

Sponsor
University of Alberta (Academic or other)
Enrollment
47 enrolled
Conditions
Overactive Bladder; Mild Cognitive Impairment
Interventions
fesoterodine 4mg; Oxybutynin; placebo; fesoterodine 8mg
Ages
older adults
Registry
NCT02240459

Full record on ClinicalTrials.gov

From the registry

The purpose of this study is to assess the effects of fesoterodine at 4mg and 8mg doses versus a placebo and oxybutynin 5mg bid versus placebo on cognitive abilities in older people with overactive bladder and mild cognitive impairment.

Primary outcomes

  • continuity of attention

History

  1. Last registry update

  2. Primary completion

  3. Started

  4. Registered

Papers citing this trial