Trials / Unknown
UnknownNCT02272322
Transvaginal Treatment of Symptomatic Cystocele Grade II-III
Transvaginal Treatment of Symptomatic Cystocele Grade II-III Using Cousin Biomesh Soft Prolaps or Allium Medical Endofast Reliant
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (estimated)
- Sponsor
- Slabbaert Koen · Academic / Other
- Sex
- Female
- Age
- 40 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
This observational study will evaluate treatment of symptomatic cystocele grade II-III with Cousin Biomesh and Allium Medical Endofast Reliant. Data about 100 patients will be collected. Follow-up till 3 years after the procedure. Primary endpoint is absence of recurrence.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | cystocele repair with biomesh soft prolaps and endofast reliant |
Timeline
- Start date
- 2014-06-01
- Primary completion
- 2017-12-01
- Completion
- 2019-12-01
- First posted
- 2014-10-22
- Last updated
- 2017-02-01
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT02272322. Inclusion in this directory is not an endorsement.