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NCT00196508 · ClinicalTrials.gov registry record · Phase 3
A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth
A Phase 3 study, sponsored by Ethicon.
- Completed
- Registry status
- Phase 3
- Development phase
- 118
- Enrollment target
NCT00196508 is a Phase 3 study that has completed, run by Ethicon. The registered enrollment target is 118 participants.
The verdict
NCT00196508, a Phase 3 study, has completed, sponsored by Ethicon.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 118 participants
- Enrollment target
Study Summary
This is a randomized controlled trial and multi-centered study with a 2-arm design. The treatment group will receive topical skin adhesive for skin closure of their wound and the control will receive sutures. Subjects will be assessed at follow-up visits. Patients are required to maintain a diary postpartum.
Interventions
- DEVICE High Viscosity DERMABOND
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 118 participants |
| Start Date | 2005-04 |
| Est. Completion | 2006-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00196508
The ClinicalTrials.gov registry entry for NCT00196508 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 118 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ethicon, which has 38 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which High Viscosity DERMABOND is the first listed.
NCT00196508 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00196508 about?
NCT00196508 is a clinical study titled "A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth". This is a randomized controlled trial and multi-centered study with a 2-arm design. The treatment group will receive topical skin adhesive for skin closure of their wound and the control will receive sutures. Subjects will be assessed at follow-up visits. Patients are required to maintain a diary po...
What is the current status of trial NCT00196508?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 118 participants. The study started on 2005-04. Estimated completion is 2006-01.
What interventions are being tested in trial NCT00196508?
The interventions under investigation include: High Viscosity DERMABOND (DEVICE).
Who is sponsoring clinical trial NCT00196508?
This trial is sponsored by Ethicon, which has 38 total clinical trials registered on ClinicalTrials.gov.
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