Clinical Trial

CLOSM Trial: Groin Closure Using Layered Option for Suture Material

Study acronym: CLOSM
Recruiting
View on ClinicalTrials.gov →
Summary
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 closure types to either groin.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-05-22; most recent amendment 2026-06-01.
Trial Details
NCT Number NCT06990425
Lead Sponsor The Cleveland Clinic
Conditions Vascular Diseases
Enrollment 259 participants
Start Date 2025-03-27
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-03