Status:
RECRUITING
CLOSM Trial: Groin Closure Using Layered Option for Suture Material
Lead Sponsor:
The Cleveland Clinic
Conditions:
Vascular Diseases
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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...
Detailed Description
Previous research has provided insights into the properties of various suture materials, yet there remains a gap in our understanding of their relative effectiveness in groin closure specifically with...
Eligibility Criteria
Inclusion
- 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
- Age 17 or younger
- Prisoners
- Pregnant patients
- Emergent cases
- Active groin infection prior to intervention
- History of prior surgical groin access (re-operative groin)
- Groin closure after extracorporeal membrane oxygenation (ECMO)
Key Trial Info
Start Date :
March 27 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2027
Estimated Enrollment :
259 Patients enrolled
Trial Details
Trial ID
NCT06990425
Start Date
March 27 2025
End Date
December 31 2027
Last Update
May 29 2025
Active Locations (1)
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1
Cleveland Clinic
Cleveland, Ohio, United States, 44195