# The Use of Dermabond Versus Standard Staple for Wound Closure in Children With Neuromuscular Scoliosis Undergoing Spinal Deformity Correction Surgery

> **NCT01135940** · PHASE2 · UNKNOWN · sponsor: **University of British Columbia** · enrollment: 80 (estimated)

## Conditions studied

- Wounds

## Interventions

- **DEVICE:** 2-octylcyanoacrylate (Dermabond) closure
- **DEVICE:** Standard staple closure

## Key facts

- **NCT ID:** NCT01135940
- **Lead sponsor:** University of British Columbia
- **Sponsor class:** OTHER
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2010-05
- **Primary completion:** 2016-06
- **Final completion:** 2016-06
- **Target enrollment:** 80 (ESTIMATED)
- **Last updated:** 2016-06-01

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01135940

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01135940, "The Use of Dermabond Versus Standard Staple for Wound Closure in Children With Neuromuscular Scoliosis Undergoing Spinal Deformity Correction Surgery". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT01135940. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
