A Study to Assess the Cognitive Effects of Fesoterodine in Elderly Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy
In brief
The study is designed to evaluate elements of cognitive function in subjects receiving either fesoterodine or alprazolam.
Key facts
- Study ID
- NCT01161472
- Run by
- Pfizer
- People needed
- 20
- Starts
- 2010-07-01
- Expected to finish
- 2010-09-01
- Last updated by the study team
- 2012-06-28
Who can join
Age: 65 and older, up to 85. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adult healthy volunteers 65 years and over with minimum MMSE of 26
You may not qualify if…
- Prohibited concomitant medications
- Confounding medical conditions
- Clinically significant comorbid diseases
- Hypersensitivity or contraindications to fesoterodine or active control
Where it is running
- Pfizer Investigational Site — Overland Park, Kansas, United States
- Pfizer Investigational Site — Overland Park, Kansas, United States
Full record on ClinicalTrials.gov
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