Aveir DR i2i Study

Status Active, not recruiting

Clinical Trial Summary

Prospective, non-randomized, multi-center, international study designed to evaluate the safety and effectiveness of the Aveir™ Dual-Chamber (DR) Leadless Pacemaker system.

Clinical Trial Description

The purpose of this clinical investigation is to evaluate the clinical safety and effectiveness of the Aveir DR Leadless Pacemaker system in a patient population indicated for a DDD(R) pacemaker. Subjects participating in the study are followed through at least 12 months with data collected at baseline, implant procedure, pre (hospital) discharge, and follow-up at 1 month, 3 months, 6 months, 12 months, and every 6 months thereafter until study completion ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05252702
Study type	Interventional
Source	Abbott Medical Devices
Contact
Status	Active, not recruiting
Phase	N/A
Start date	February 2, 2022
Completion date	November 2025

View Details

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