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Clinical trial

A Post-Market Evaluation of the Altis® Single Incision Sling System Versus Transobturator or Retropubic Mesh Sling in the Treatment of Female Stress Urinary Incontinence

NCT02348112 is registered in ClinicalTrials.gov with Coloplast A/S as lead sponsor.

NCT NCT02348112
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Registry record

As filed in ClinicalTrials.gov.

Title
A Post-Market Evaluation of the Altis® Single Incision Sling System Versus Transobturator or Retropubic Mesh Sling in the Treatment of Female Stress Urinary Incontinence
Lead sponsor
Coloplast A/S
Phase
Observational
Overall status
Completed
Start date
January 31, 2015
Completion date
September 30, 2021
Enrollment
416 (actual)
Sites
27

Conditions

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

stress urinary incontinence