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Instrumental Sealing of Arterial Puncture Site Closure Device Versus Manual Compression Trial

NCT01389375 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 4524

Last updated 2016-06-10

No results posted yet for this study

Summary

Are novel vascular closure devices noninferior to manual compression regarding access site complications after coronary angiography?

Conditions

Interventions

DEVICE

FemoSeal®

Closure device for femoral artery access closure

DEVICE

ExoSeal®

Closure device for femoral artery access closure

OTHER

Manual compression

Conventional manual compression

Sponsors & Collaborators

  • Deutsches Herzzentrum Muenchen

    lead OTHER

Principal Investigators

  • Maryam Linhardt, MD · Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

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 NCT01389375 on ClinicalTrials.gov