MedTrace Logo

Mynx M5 One Hour Ambulation Study

NCT01100476 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2013-02-15

No results posted yet for this study

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

Conditions

  • Angiography

Interventions

DEVICE

Endovascular Diagnostic Procedures

Patients underwent a percutaneous diagnostic procedure utilizing a 5F procedural sheath in the common femoral artery

Sponsors & Collaborators

  • AccessClosure, Inc.

    collaborator INDUSTRY

  • Cardiovascular Associates of the Delaware Valley

    lead OTHER

Principal Investigators

  • Vijay K Verma, MD · Cardiovascular Associates of the Delaware Valley

  • Mary F Kinder, RN, BSN · Cardiovascular Associates of the Delaware Valley

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2011-08-31
Completion
2011-08-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01100476 on ClinicalTrials.gov