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Clinical Trial

Early Feasibility Study of 3830 Lead Implantation Via the Middle Cardiac Vein in Patients With Prior or Planned Tricuspid Valve Intervention

NCT: NCT07805525 · NOT_YET_RECRUITING

NCT IDNCT07805525
StatusNOT_YET_RECRUITING
SponsorMinneapolis Heart Institute Foundation (OTHER)
First posted
Last updated

Brief Summary

Prospective, single center, early feasibility study designed to evaluate the initial safety and device performance of the Medtronic 3830 Lead when implanted via the Middle Cardiac Vein in patients with prior or planned tricuspid valve interventions.

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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