Trials / Completed
CompletedNCT02547077
Use of 2-octylcyanoacrylate (Dermabond) Versus 5-0 Fast Absorbing Gut During Cutaneous Wound Closure
Use of 2-octylcyanoacrylate (Dermabond) Versus 5-0 Fast Absorbing Gut During Cutaneous Wound Closure: a Randomized Evaluator Blinded Split Wound Comparative Effectiveness Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- University of California, Davis · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether the use of 2-octylcyanoacrylate during repair of linear cutaneous surgery wounds improves scar cosmesis compared to wound closure with 5-0 fast absorbing gut.
Detailed description
The purpose of this study is to determine whether the use of 2-octylcyanoacrylate during repair of linear cutaneous surgery wounds improves scar cosmesis compared to wound closure with 5-0 fast absorbing gut. The investigators will use a split wound model, where half of the wound is treated with 2-octylcyanoacrylate and the other half is repaired with 5-0 fast absorbing gut. Three-months post-surgery, the scar will be measured via the physician observer scar assessment scale, a validated scar instrument. The scar width, and adverse events will also be recorded.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Wound Closure with 2-octylcyanoacrylate | |
| PROCEDURE | Wound Closure with 5-0 Fast Absorbing Gut Sutures |
Timeline
- Start date
- 2015-07-01
- Primary completion
- 2015-12-01
- Completion
- 2016-05-01
- First posted
- 2015-09-11
- Last updated
- 2017-05-30
Source: ClinicalTrials.gov record NCT02547077. Inclusion in this directory is not an endorsement.