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Clinical Trial

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

NCT: NCT03923387 · COMPLETED

NCT IDNCT03923387
StatusCOMPLETED
Start Date2019-04-24
Completion2020-10-22
SponsorCordis US Corp. (INDUSTRY)
First posted
Last updated

Brief 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.

Frequently Asked Questions

What is Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device?

Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device is a clinical trial registered under NCT03923387. Current status: COMPLETED.

What is the status of NCT03923387?

The current status of NCT03923387 (Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device) is: COMPLETED.

When did Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device start?

Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device started on 2019-04-24.

Related Devices

PMA P040044Device, hemostasis, vascularCordis US Corporation PMA P100013Device, hemostasis, vascularCordis US Corporation PMA P120002STENT, SUPERFICIAL FEMORAL ARTERYCordis US Corporation K221832SABER .014 PTA Dilatation Catheter; SABERX .014 PTA Dilatation CatheterCordis US Corp K230704RAIN Sheath™ Tibial Pedal IntroducerCordis US Corp

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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