# 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** · — · COMPLETED · sponsor: **Cousin Biotech** · enrollment: 290 (actual)

## Conditions studied

- Prolapse; Female

## Interventions

- **PROCEDURE:** promontofixation, prolapse cure

## Key facts

- **NCT ID:** NCT06620211
- **Lead sponsor:** Cousin Biotech
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2020-04-23
- **Primary completion:** 2023-10-19
- **Final completion:** 2023-10-19
- **Target enrollment:** 290 (ACTUAL)
- **Last updated:** 2024-10-01


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06620211

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06620211, "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.". Retrieved via AI Analytics 2026-07-25 from https://api.ai-analytics.org/clinical/NCT06620211. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*