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Patient Preferences for Leadless Pacemakers

NCT05327101 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 117

Last updated 2025-02-20

Study results available
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Summary

Prospective, non-randomized, multi-center study designed to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers

Conditions

  • Cardiac Rhythm Disorder
  • Bradycardia
  • Cardiac Pacemaker Artificial

Interventions

OTHER

Patient Preference Survey

Patient preference survey on implantable cardiac pacemaker systems

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Shelby Reed, PhD · Duke Clinical Research Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-28
Primary Completion
2023-06-13
Completion
2023-06-13

Countries

  • United States

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 NCT05327101 on ClinicalTrials.gov