# Multicenter, Prospective, Non-randomized, Single-arm, Interventional Study for the Evaluation of the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse

> **NCT03195361** · NA · COMPLETED · sponsor: **Lyra Medical Ltd.** · enrollment: 50 (estimated)

## Conditions studied

- Anterior Vaginal Wall Prolapse With/Without Apical/Uterine Descent

## Interventions

- **DEVICE:** SRS - Self Retaining Support system

## Key facts

- **NCT ID:** NCT03195361
- **Lead sponsor:** Lyra Medical Ltd.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2016-03
- **Primary completion:** 2020-12-20
- **Final completion:** 2020-12-20
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2021-02-03


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03195361

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03195361, "Multicenter, Prospective, Non-randomized, Single-arm, Interventional Study for the Evaluation of the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT03195361. Licensed CC0.

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