CLOSM Trial: Groin Closure Using Layered Option for Suture Material
This study, called the CLOSM trial, is looking at the best way to close groin incisions (cuts) after vascular surgery. Researchers are comparing two different types of stitches: PDS (polydioxanone) suture and Vicryl suture. The goal is to see which type of stitch leads to fewer complications in the groin area. You might be able to join if you are over 18 and having planned (elective) vascular surgery that requires a groin incision. If you have incisions on both sides, one side might get PDS and the other Vicryl. The main thing they'll be looking at is the rate of groin complications after 30 days and after 1 year. The current status of this study is unclear, but it plans to enroll 259 participants.
- Study design
- This is a randomized controlled trial comparing two types of sutures. About 259 participants will be randomly assigned to receive either PDS or Vicryl suture for their groin closure.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed to check for groin complications at 30 days and 1 year after surgery.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
CLOSM Trial: Groin Closure Using Layered Option for Suture Material
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Francis Caputo, MD · PRINCIPAL_INVESTIGATOR · The Cleveland Clinic
Who to contact
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Do you actually qualify for this trial?
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Inclusion
What this trial measures
- Rate of groin complication30 days and 1 year
Number of occurrence of the access site complication