Mobilization and Outcomes After Venous Closure

Recruiting now

Conditions studied: Venous Vascular Closure, Electrophysiology Study

In brief

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.

Key facts

Study ID

NCT07246902

Run by

Cordis US Corp.

People needed

300

Starts

2025-11-24

Expected to finish

2026-08-01

Last updated by the study team

2026-03-16

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Able and willing to provide informed consent and to complete a follow-up visit at 14 ± 7 days post-procedure.
• Individuals undergoing catheter-based procedures utilizing 6F to 12F inner diameter procedural sheaths, with single or multiple venous access sites in one or both limbs.
• Individuals who are candidates to have their venous access site(s) closed with MYNX CONTROL™ VENOUS VCD 6F-12F per IFU.
• At the time of enrollment, the Investigator deems the subject a candidate for same-day discharge (SDD) per standard of care (no procedure related events/complications e.g., no new pericardial effusion, post-procedure diuresis not needed, etc.).

You may not qualify if…

• Presence of bruit, palpable aneurysm, significant candida or groin infection.
• Prior to closure, presence of hematoma in the accessed limb.
• Currently involved in any other clinical trial that may interfere with the outcomes of this study as determined by the Investigator.
• Planned use of other closure devices or techniques other than MYNX CONTROL™ VENOUS VCD 6F-12F.
• Life expectancy <12 months.

Where it is running

• South Denver Cardiology — Littleton, Colorado, United States (enrolling)
• KC Heart and Rhythm Institute — Overland Park, Kansas, United States (enrolling)
• North Carolina Heart & Vascular Research, LLC — Raleigh, North Carolina, United States (enrolling)

Full record on ClinicalTrials.gov

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