Clinical trial
A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy…
NCT00196508 · Ethicon, Inc., Industry · Completed
Key facts
| NCT number | NCT00196508 |
|---|---|
| Title | A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth |
| Official title | A Randomized, Multi Center Study to Evaluate the Clinical Performance of Topical Skin Adhesive in Comparison to Sutures for Perineal Skin Closure Following Childbirth |
| Lead sponsor | Ethicon, Inc., Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Episiotomy, Perineal Tear |
| Intervention type | Device |
| Interventions | High Viscosity DERMABOND |
| Enrollment | 118 |
| Start date | Apr 1, 2005 |
| Completion | Jan 1, 2006 |
| First posted | Sep 20, 2005 |
| Last update posted | Oct 16, 2007 |
| Countries | United States |
At a glance
- 1–9 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: