Trials / Completed
CompletedNCT02190825
Safety and Efficacy Study of the NeuGuide Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 15 (actual)
- Sponsor
- Pop Medical Solutions · Industry
- Sex
- Female
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to investigate the safety, efficacy, peri and postoperative complications, and patient satisfaction of sacro-spinous ligament fixation (SSLF) for the management of pelvic organ prolapse (POP). Prolapse staging for all subjects in this study will be performed according to the POP-Q staging system. Ultrasound examinations for all subjects in this study are subjected to the surgeon need and will be performed if required by qualified personnel
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | NeuGuide device | The NeuGuideTM device is indicated for anchoring sutures to ligaments of the pelvic floor |
Timeline
- Start date
- 2014-11-01
- Primary completion
- 2016-04-01
- Completion
- 2023-10-30
- First posted
- 2014-07-15
- Last updated
- 2023-11-22
Locations
2 sites across 1 country: Israel
Source: ClinicalTrials.gov record NCT02190825. Inclusion in this directory is not an endorsement.