Actively Recruiting
Mobilization and Outcomes After Venous Closure
Led by Cordis US Corp. · Updated on 2026-03-16
300
Participants Needed
3
Research Sites
35 weeks
Total Duration
On this page
Sponsors
C
Cordis US Corp.
Lead Sponsor
N
NAMSA
Collaborating Sponsor
AI-Summary
What this Trial Is About
The primary objective of this post-market registry is to collect real-world outcomes and evaluate usage practice of MYNX CONTROL™ VENOUS (MCV) Vascular Closure Device (VCD) 6F-12F in sealing femoral venous access sites in patients who have undergone endovascular procedures in a real-world setting.
CONDITIONS
Official Title
Mobilization and Outcomes After Venous Closure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able and willing to provide informed consent and complete a follow-up visit at 14 �b1 7 days post-procedure
- Undergoing catheter-based procedures using 6F to 12F inner diameter procedural sheaths with one or more venous access sites in one or both limbs
- Eligible to have venous access sites closed with MYNX CONTROL174; VENOUS VCD 6F-12F according to instructions for use
- Considered by the Investigator to be a candidate for same-day discharge without procedure-related complications at enrollment
You will not qualify if you...
- Presence of bruit, palpable aneurysm, or significant candida or groin infection
- Hematoma present in the accessed limb before closure
- Currently participating in another clinical trial that could affect this study's outcomes
- Planned use of other closure devices or techniques instead of MYNX CONTROL174; VENOUS VCD 6F-12F
- Life expectancy less than 12 months
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
South Denver Cardiology
Littleton, Colorado, United States, 80210
Actively Recruiting
2
KC Heart and Rhythm Institute
Overland Park, Kansas, United States, 66211
Actively Recruiting
3
North Carolina Heart & Vascular Research, LLC
Raleigh, North Carolina, United States, 27607
Actively Recruiting
Research Team
R
Rajesh Nathan
CONTACT
J
Jennifer Lee
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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