Trials / Completed
CompletedNCT01244165
Study of Cytrix Use in Pelvic Floor Prolapse Treatment
Clinical Investigation of Fetal Bovine Dermis Material (Cytrix) for Use in the Treatment of Pelvic Floor Prolapse
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 45 (actual)
- Sponsor
- Boston Scientific Corporation · Industry
- Sex
- Female
- Age
- 30 Years – 85 Years
- Healthy volunteers
- Accepted
Summary
To evaluate safety and effectiveness of using the fetal bovine dermis (Cytrix) in the treatment of pelvic organ prolapse.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Cytrix | |
| OTHER | Other treatments for pelvic organ prolapse | Treatments for pelvic organ prolapse using other products (standard of care for treatment of pelvic organ prolapse) |
Timeline
- Start date
- 2002-01-01
- Primary completion
- 2006-10-01
- Completion
- 2006-10-01
- First posted
- 2010-11-19
- Last updated
- 2010-11-19
Source: ClinicalTrials.gov record NCT01244165. Inclusion in this directory is not an endorsement.