Trials / Completed
CompletedNCT03195361
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
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Lyra Medical Ltd. · Industry
- Sex
- Female
- Age
- 50 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
A prospective, single arm, multi-center clinical study to evaluate the safety and performance of the SRS (Lyra Medical) vaginal mesh in POP patients
Detailed description
The SRS implant is intended for transvaginal surgical treatment of anterior vaginal wall prolapse with or without vaginal apex/uterine prolapses
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SRS - Self Retaining Support system |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2020-12-20
- Completion
- 2020-12-20
- First posted
- 2017-06-22
- Last updated
- 2021-02-03
Locations
3 sites across 1 country: Israel
Source: ClinicalTrials.gov record NCT03195361. Inclusion in this directory is not an endorsement.