Clinical trial
The Maximum Tolerated Dose and Minimum Effective Dose of OROS® Oxybutynin Compared to Ditropan® (Immediate-release Oxybutynin) in the Treatment of Patients With Urge or Mixed Urinary Incontinence
NCT00269750 is registered in ClinicalTrials.gov with Alza Corporation, DE, USA as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- The Maximum Tolerated Dose and Minimum Effective Dose of OROS® Oxybutynin Compared to Ditropan® (Immediate-release Oxybutynin) in the Treatment of Patients With Urge or Mixed Urinary Incontinence
- Lead sponsor
- Alza Corporation, DE, USA
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- July 31, 1996
- Completion date
- February 28, 1997
- Enrollment
- 100
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
urge incontinence