Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device — PANDA

Endovascular Clinical Trial

Official title:
A Multicenter, Open Label, Prospective, Randomized Study of the MynxGrip Vascular Closure Device in Subjects With Diagnostic or Interventional Endovascular Procedures (PANDA Study)

Status Completed

Clinical Trial Summary

To evaluate the safety and effectiveness of MynxGrip, in hemostasis of common femoral artery puncture site, compared with manual compression hemostasis in patients who have undergone diagnostic or interventional endovascular procedures utilizing a 5F, 6F or 7F procedural sheath.

Clinical Trial Description

Effectiveness: to superiority to the control group in time to hemostasis. Comparison of time to ambulation, procedure success rate, length of stay in hospital, device success rate. Safety-Major/Minor complication rate, adverse events, SAEs as compared to control. ;

Study Design

Related Conditions & MeSH terms

Endovascular

Clinical Trial Details

NCT number	NCT03923387
Study type	Interventional
Source	Cordis Corporation
Contact
Status	Completed
Phase	N/A
Start date	May 7, 2019
Completion date	September 1, 2020

View Details

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