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Vascular Closure Device in Transcatheter Aortic Valve Replacement

NCT04392492 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2020-12-02

No results posted yet for this study

Summary

Evaluation of the safety and efficacy of a percutaneous plug-based large-bore vascular closure device for femoral artery closure in an unselected consecutive patient cohort undergoing transcatheter aortic valve implantation in a single-center prospective study.

Conditions

  • Aortic Valve Stenosis

Interventions

DEVICE

MANTA vascular closure device

Femoral access site closure using the MANTA closure device

Sponsors & Collaborators

  • Karolinska University Hospital

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-25
Primary Completion
2020-12-31
Completion
2021-01-31
FDA Device
Yes

Countries

  • Sweden

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 NCT04392492 on ClinicalTrials.gov