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RECRUITING
NCT06990425
NA

CLOSM Trial: Groin Closure Using Layered Option for Suture Material

Sponsor: The Cleveland Clinic

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

259

Start Date

2025-03-27

Completion Date

2027-12-31

Last Updated

2025-05-29

Healthy Volunteers

No

Interventions

PROCEDURE

Groin closure with PDS suture

Closure of the groin will be performed with PDS suture

PROCEDURE

Groin closure suture material

Closure of the groin will be performed with Vicryl suture

Locations (1)

Cleveland Clinic

Cleveland, Ohio, United States