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NCT06990425 · ClinicalTrials.gov registry record · NA
CLOSM Trial: Groin Closure Using Layered Option for Suture Material
A NA study of Vascular Diseases, sponsored by The Cleveland Clinic.
- Recruiting
- Registry status
- NA
- Development phase
- 259
- Enrollment target
- 1
- Study location
NCT06990425 is a NA study of Vascular Diseases that is actively recruiting participants, run by The Cleveland Clinic. The registered enrollment target is 259 participants, below the 555-participant average among 40 other Vascular Diseases trials with a reported enrollment target (53% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06990425, a NA study of Vascular Diseases, is actively recruiting participants, sponsored by The Cleveland Clinic.
- RECRUITING
- Registry status
- NA
- Development phase
- 259 participants
- Enrollment target
- 1
- Study location
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 Studied
Interventions
- PROCEDURE Groin closure with PDS suture
- PROCEDURE Groin closure suture material
Study Locations (1)
Ohio
- Cleveland Clinic - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 259 participants |
| Start Date | 2025-03-27 |
| Est. Completion | 2027-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06990425
The ClinicalTrials.gov registry entry for NCT06990425 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 259 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 555-participant average among 40 other Vascular Diseases trials with a reported enrollment target (53% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Vascular Diseases appearing as the primary indexed condition, and to 2 interventions - of which Groin closure with PDS suture is the first listed.
NCT06990425 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT06990425 about?
NCT06990425 is a clinical study titled "CLOSM Trial: Groin Closure Using Layered Option for Suture Material". 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...
What is the current status of trial NCT06990425?
This trial is currently recruiting. It is a NA study. The enrollment target is 259 participants. The study started on 2025-03-27. Estimated completion is 2027-12-31.
What conditions does trial NCT06990425 study?
This clinical trial studies the following conditions: Vascular Diseases.
What interventions are being tested in trial NCT06990425?
The interventions under investigation include: Groin closure with PDS suture (PROCEDURE), Groin closure suture material (PROCEDURE).
Who is sponsoring clinical trial NCT06990425?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06990425 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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