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The Sentinel Registry

NCT05217888 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 158

Last updated 2025-06-13

No results posted yet for this study

Summary

This registry is to evaluate procedural outcomes and safety outcomes of cerebral protection devices during transfemoral TAVR in real-world clinical practice.

The data from this registry will be compared with the extracted data from the TP TAVR registry(NCT038262664) using Propensity Score Matching.

Conditions

  • Aortic Valve Disease
  • Transcatheter Aortic Valve Implantation
  • Transcatheter Aortic Valve Replacement

Interventions

DEVICE

Sentinel

cerebral protection devices during transfemoral transcatheter aortic valve replacement

Sponsors & Collaborators

  • CardioVascular Research Foundation, Korea

    collaborator OTHER

  • Boston Scientific Corporation

    collaborator INDUSTRY

  • Duk-Woo Park, MD

    lead OTHER

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-18
Primary Completion
2025-05-20
Completion
2025-05-20

Countries

  • South Korea

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 NCT05217888 on ClinicalTrials.gov