Clinical trial
Safety Study of Pelvic Organ Prolapse Repair Using Transvaginal Mesh
NCT00402844 · Karolinska Institutet, Other · Completed
Key facts
| NCT number | NCT00402844 |
|---|---|
| Title | Safety Study of Pelvic Organ Prolapse Repair Using Transvaginal Mesh |
| Official title | A Multicenter Clinical Safety Assessment of Polypropylene Transvaginal Mesh in Pelvic Reconstructive Surgery |
| Lead sponsor | Karolinska Institutet, Other |
| Collaborators | Karolinska University Hospital |
| Status | Completed |
| Phase | Phase 2/Phase 3 |
| Study type | Interventional |
| Conditions | Pelvic Organ Prolapse |
| Intervention type | Device |
| Interventions | Transvaginal mesh- PROLIFT®-system |
| Enrollment | 250 |
| Start date | Aug 1, 2006 |
| Completion | Mar 1, 2007 |
| First posted | Nov 22, 2006 |
| Last update posted | Nov 14, 2007 |
| Countries | Denmark, Finland, Norway, Sweden |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: