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NCT07246902 · ClinicalTrials.gov registry record

Mobilization and Outcomes After Venous Closure

A clinical trial of Electrophysiology Study and Venous Vascular Closure, sponsored by Cordis US.

Recruiting
Registry status
300
Enrollment target
3
Study locations

NCT07246902 is a study of Electrophysiology Study and Venous Vascular Closure that is actively recruiting participants, run by Cordis US. The registered enrollment target is 300 participants. The trial reports 3 study locations across 3 states.

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The verdict

NCT07246902, a study of Electrophysiology Study and Venous Vascular Closure, is actively recruiting participants, sponsored by Cordis US.

RECRUITING
Registry status
300 participants
Enrollment target
3
Study locations

Study Summary

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.

Interventions

  • DEVICE MYNX CONTROLTM VENOUS Vascular Closure Device

Study Locations (3)

Colorado

  • South Denver Cardiology - Littleton

Kansas

  • KC Heart and Rhythm Institute - Overland Park

North Carolina

  • North Carolina Heart & Vascular Research, LLC - Raleigh

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2025-11-24
Est. Completion 2026-08

Sponsor

Cordis US

19 total trials

What the Registry Record Tells You About NCT07246902

The ClinicalTrials.gov registry entry for NCT07246902 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cordis US, which has 19 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Electrophysiology Study appearing as the primary indexed condition, and to 1 intervention - of which MYNX CONTROLTM VENOUS Vascular Closure Device is the first listed.

NCT07246902 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Colorado, Kansas, North Carolina.

Frequently Asked Questions

What is clinical trial NCT07246902 about?

NCT07246902 is a clinical study titled "Mobilization and Outcomes After Venous Closure". 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.

What is the current status of trial NCT07246902?

This trial is currently recruiting. The enrollment target is 300 participants. The study started on 2025-11-24. Estimated completion is 2026-08.

What conditions does trial NCT07246902 study?

This clinical trial studies the following conditions: Electrophysiology Study, Venous Vascular Closure.

What interventions are being tested in trial NCT07246902?

The interventions under investigation include: MYNX CONTROLTM VENOUS Vascular Closure Device (DEVICE).

Who is sponsoring clinical trial NCT07246902?

This trial is sponsored by Cordis US, which has 19 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07246902 being conducted?

This trial has 3 study locations across Colorado, Kansas, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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