Vicryl Rapide Versus Nonabsorbable Suture
Recruiting
N/A
Interventional Study
Traumatic Lacerations
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 96 (estimated)
- Sponsor
- University of California, San Francisco · Other
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About This Trial
This will be a prospective, randomized controlled trial assessing noninferiority of Vicryl Rapide compared to nonabsorbable suture. The study will be conducted in the Community Regional Medical Center emergency department (ED). The aim of this study, then, is to prospectively determine if 3-month cosmesis for traumatic laceration repair of trunk/extremity lacerations in adult patients with Vicryl …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient 18-years or older
* single laceration on trunk or extremity requiring suture closure
* laceration length \> 2-cm
* wound to be closed with simple interrupted sutures
Exclusion Criteria:
* High infection potential
* Must have one of the following:
* puncture…
Contacts