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Mynx M5 One Hour Ambulation Study — Mynx  

Angiography Clinical Trial

Official title:
Single-center, Post Market, Prospective, Consecutive, Single-arm Study Compared to Historical Control (Diagnostic Arm of the Mynx 6/7F Study)

Clinical Trial Summary

The Mynx Vascular Closure Device (Mynx M5) is a sponge-like material used to close the hole in the artery after patients undergo a diagnostic endovascular procedures

Clinical Trial Description

Key Inclusion:

1. Patients >18 yrs of age

2. Patient underwent a percutaneous diagnostic procedure utilizing a 5F procedural sheath via the common femoral artery.

3. Patient is able to ambulate (routinely walk 6 meters or 20 feet without assistance for any reason) as assessed by investigator. ;

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01100476
Study type Interventional
Source Cardiovascular Associates of the Delaware Valley
Contact
Status Completed
Phase Phase 4
Start date March 2010
Completion date August 2011
View Details
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