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Clinical trial

Evaluation of the Safety, Performance, and Tolerability of the Sacromesh® Medical Device in the Treatment of Prolapse by Promontofixation in a Population of Patients Followed Over the Long Term.

NCT06620211 is registered in ClinicalTrials.gov with Cousin Biotech as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Evaluation of the Safety, Performance, and Tolerability of the Sacromesh® Medical Device in the Treatment of Prolapse by Promontofixation in a Population of Patients Followed Over the Long Term.
Lead sponsor
Cousin Biotech
Phase
Observational
Overall status
Completed
Start date
April 23, 2020
Completion date
October 19, 2023
Enrollment
290 (actual)
Sites
1

Conditions

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

prolapse; female