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CLOSM Trial: Groin Closure Using Layered Option for Suture Material

NCT06990425 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 259

Last updated 2026-06-03

No results posted yet for this study

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.

Conditions

  • Vascular Diseases

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

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Principal Investigators

  • Francis Caputo, MD · The Cleveland Clinic

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-27
Primary Completion
2027-12-31
Completion
2027-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06990425 on ClinicalTrials.gov