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Clinical Trial

Lead Evaluation for Defibrillation and Reliability Post Approval Study

NCT: NCT07005232 · ENROLLING_BY_INVITATION

NCT IDNCT07005232
StatusENROLLING_BY_INVITATION
Start Date2026-01-07
SponsorMedtronic (INDUSTRY)
First posted
Last updated

Brief Summary

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).

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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