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Study identifier: NCT07005232 Synced from ClinicalTrials.gov · August 03, 2026
● Enrolling By Invitation

Lead Evaluation for Defibrillation and Reliability Post Approval Study

Condition: Tachyarrhythmia  ·  Sponsor: Medtronic

PhaseN/A
Planned participants2000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

Medtronic is sponsoring the LEADR PAS to provide continuing evaluation and periodic reporting of safety and effectiveness of the OmniaSecure™ defibrillation lead following commercial release. The LEADR PAS is conducted within Medtronic's Product Surveillance Registry Platform (NCT01524276).

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (73)

The University of Alabama at BirminghamBirmingham, Alabama, United States
Stanford Hospital & ClinicsStanford, California, United States
COR HealthcareTorrance, California, United States
Childrens Hospital ColoradoAurora, Colorado, United States
Hartford HosptialHartford, Connecticut, United States
Childrens National Medical CenterWashington D.C., District of Columbia, United States
Heart Rhythm SolutionsHollywood, Florida, United States
Cardiovascular Institute of Northwest FloridaPanama City, Florida, United States
Heart & Vascular Institute of FloridaSafety Harbor, Florida, United States
Intercoastal Medical GroupSarasota, Florida, United States
University of South Florida Health (USF)Tampa, Florida, United States
WellStar Research InstituteMarietta, Georgia, United States

+ 61 more locations — full list on the registry record.

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