Trials / Completed
CompletedNCT02209337
Demonstrate the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Lyra Medical Ltd. · Industry
- Sex
- Female
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
A prospective, single arm, pre-market, multi-center clinical study to evaluate the safety and performance of the SRS (Lyra Medical) vaginal mesh in POP patients
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SRS |
Timeline
- Start date
- 2014-09-01
- Primary completion
- 2016-03-01
- Completion
- 2018-03-01
- First posted
- 2014-08-05
- Last updated
- 2019-08-16
Locations
3 sites across 2 countries: Hungary, Israel
Source: ClinicalTrials.gov record NCT02209337. Inclusion in this directory is not an endorsement.