# Demonstrate the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse

> **NCT02209337** · NA · COMPLETED · sponsor: **Lyra Medical Ltd.** · enrollment: 20 (actual)

## Conditions studied

- Anterior Vaginal Wall Prolapse
- Vaginal Apex/Uterine Prolapse

## Interventions

- **DEVICE:** SRS

## Key facts

- **NCT ID:** NCT02209337
- **Lead sponsor:** Lyra Medical Ltd.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2014-09
- **Primary completion:** 2016-03
- **Final completion:** 2018-03
- **Target enrollment:** 20 (ACTUAL)
- **Last updated:** 2019-08-16


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02209337

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02209337, "Demonstrate the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT02209337. Licensed CC0.

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