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.
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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

Brian Chinnock, MD

559-499-6440

bchinnock@fresno.ucsf.edu

CONTACT

Jannet Castaneda, BA

559-994-5893

jcastaneda@fresno.ucsf.edu

CONTACT