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Clinical trial

Post-approval of Coaptite® in the Treatment of Female Urinary Incontinence

NCT00996489 is registered in ClinicalTrials.gov with Merz North America, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Post-approval of Coaptite® in the Treatment of Female Urinary Incontinence
Lead sponsor
Merz North America, Inc.
Phase
Not applicable
Overall status
Completed
Start date
January 8, 2008
Completion date
November 2, 2015
Enrollment
459 (actual)
Sites
20

Conditions

As the registry lists them; a condition with its own page is linked.

female stress urinary incontinence due to intrinsic sphincter deficiency