CLOSM Trial: Groin Closure Using Layered Option for Suture Material
Recruiting
N/A
Interventional Study
Vascular Diseases
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
- 259 (estimated)
- Sponsor
- The Cleveland Clinic · Other
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About This Trial
This is a randomized controlled trial comparing groin closure after vascular intervention with Vicryl suture versus PDS (polydioxanone) suture. This will be a single center trail performed at CCF main campus. Patients will be enrolled in a prospective fashion and will be randomized 1:1 to either PDS or Vicryl closure. Patients undergoing bilateral groin exposure will be randomized to receive both …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All patients \> 18 years who undergo ELECTIVE vascular surgery that would require groin incisions
* Patients with to undergo ELECTIVE bilateral groin incisions will be matched to receive closure with PDS in one groin and Vicryl in the other groin
Exclusion Criteria:
1. Age 1…
Contacts