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Clinical Trial

A 3 Years Naturalistic Cohort Survey of Altis Single Incision Sling System For Female Stress Urinary Incontinence

NCT: NCT04115605 · TERMINATED

NCT IDNCT04115605
StatusTERMINATED
Start Date2015-05-23
Completion2022-06-24
SponsorColoplast A/S (INDUSTRY)
First posted
Last updated

Brief Summary

The purpose of this study is to monitor the use of Altis Single Incision Sling (SIS) in a real world population and collect medical data on effectiveness and to monitor safety of Altis SIS at 12 and 36 months post device implantation in women with stress urinary incontinence.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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