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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