Condition: Vascular Diseases · Sponsor: The Cleveland Clinic
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.
This description comes directly from the study's public registry record.
Ahmed Sorour, MD · 216-399-9224 · SOROURA2@ccf.org
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| Cleveland Clinic | Cleveland, Ohio, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06990425