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Randomized Comparison of MynxGrip Vascular Closure Device and Manual Compression for Closure After Femoral Access Angiography. The Closure Devices Used in Every Day Practice Study, CLOSE-UP III Trial

NCT02237430 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 869

Last updated 2019-05-08

No results posted yet for this study

Summary

Is the MynxGrip (test device) non-inferior to manuel compression (standard comparator) in the incidence of adverse access site related events in-hospital, at 30 days and at 6 months.

Conditions

  • Coronary Disease

Interventions

DEVICE

MynxGrip

Closure device for femoral artery access closure

OTHER

Manual compression

Conventional manual compression

Sponsors & Collaborators

  • Vingmed Danmark A/S

    collaborator INDIV

  • Aarhus University Hospital Skejby

    lead OTHER

Principal Investigators

  • Evald H Christiansen, MD · Aarhus University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-16
Primary Completion
2017-05-16
Completion
2018-12-16

Countries

  • Denmark

Study Locations

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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 NCT02237430 on ClinicalTrials.gov