Clinical Trial to Evaluate the Efficacy and Safety of Fesoterodine in Comparison to Tolterodine for Overactive Bladder (OAB)
Completed · Phase 3 · Has a placebo group
Conditions studied: Overactive Bladder
In brief
To evaluate the efficacy and safety of fesoterodine in comparison to tolterodine and placebo for overactive bladder
Key facts
- Study ID
- NCT00444925
- Run by
- Pfizer
- People needed
- 1712
- Starts
- 2007-04-01
- Expected to finish
- 2008-07-01
- Last updated by the study team
- 2015-03-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult overactive bladder (OAB) patients who present with OAB symptoms, including urinary frequency >= 8 per day and urgency urinary incontinence >=1 per day
You may not qualify if…
- Patients with conditions that would contraindicate for fesoterodine use, e.g, hypersensitivity to the active substance (fesoterodine) or to peanut or soya or any of the excipients, urinary retention, and gastric retention.
- Patients with significant hepatic and renal disease or other significant unstable diseases.
- OAB symptoms caused by neurological conditions, known pathologies of urinary tract, etc.
Where it is running
- Pfizer Investigational Site — Huntsville, Alabama, United States
- Pfizer Investigational Site — Mobile, Alabama, United States
- Pfizer Investigational Site — Carmichael, California, United States
- Pfizer Investigational Site — Orangevale, California, United States
- Pfizer Investigational Site — San Diego, California, United States
- Pfizer Investigational Site — Aurora, Colorado, United States
- Pfizer Investigational Site — Waterbury, Connecticut, United States
- Pfizer Investigational Site — Miami, Florida, United States
- Pfizer Investigational Site — Wellington, Florida, United States
- Pfizer Investigational Site — Atlanta, Georgia, United States
- Pfizer Investigational Site — Coeur d'Alene, Idaho, United States
- Pfizer Investigational Site — Sandpoint, Idaho, United States
- Pfizer Investigational Site — Aurora, Illinois, United States
- Pfizer Investigational Site — West Des Moines, Iowa, United States
- Pfizer Investigational Site — Newton, Kansas, United States
- Pfizer Investigational Site — Shrevport, Louisiana, United States
- Pfizer Investigational Site — Watertown, Massachusetts, United States
- Pfizer Investigational Site — Chaska, Minnesota, United States
- Pfizer Investigational Site — Lawrenceville, New Jersey, United States
- Pfizer Investigational Site — Albuquerque, New Mexico, United States
- Pfizer Investigational Site — Garden City, New York, United States
- Pfizer Investigational Site — Mineola, New York, United States
- Pfizer Investigational Site — Burlington, North Carolina, United States
- Pfizer Investigational Site — Concord, North Carolina, United States
- Pfizer Investigational Site — Homewood, Alabama, United States
Full record on ClinicalTrials.gov
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