# A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth

> **NCT00196508** · PHASE3 · COMPLETED · sponsor: **Ethicon, Inc.** · enrollment: 118 (—)

## Conditions studied

- Episiotomy
- Perineal Tear

## Interventions

- **DEVICE:** High Viscosity DERMABOND

## Key facts

- **NCT ID:** NCT00196508
- **Lead sponsor:** Ethicon, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2005-04
- **Primary completion:** —
- **Final completion:** 2006-01
- **Target enrollment:** 118 (—)
- **Last updated:** 2007-10-16


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00196508

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00196508, "A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT00196508. Licensed CC0.

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