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Medtronic HAMMOCK Post Approval Study

NCT03139721 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 122

Last updated 2024-08-23

Study results available
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Summary

This study is being conducted to satisfy the post-CE approval requirement.

Conditions

  • Heart Valve Diseases

Interventions

DEVICE

Mosaic model 305, model 310, and ultra model 305

Aortic or mitral valve replacement

Sponsors & Collaborators

  • Medtronic Cardiac Surgery

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-19
Primary Completion
2019-05-17
Completion
2021-06-21
FDA Device
Yes

Countries

  • United States
  • Germany
  • Poland

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 NCT03139721 on ClinicalTrials.gov