Follow-up Registry to Monitor the Efficacy and Safety of the Occlutech PLD Device

NCT03003481 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 144

Last updated 2022-04-20

No results posted yet for this study

Summary

Collect patient data and to monitor the clinical use (safety and efficacy) of the device

Conditions

  • Mitral Paravalvular Leaks (PVL)
  • Aortic Paravalvular Leaks (PVL)

Sponsors & Collaborators

  • Occlutech International AB

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-31
Primary Completion
2021-05-31
Completion
2021-05-31

Countries

  • Italy

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 NCT03003481 on ClinicalTrials.gov