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Leadless Pacemaker Registry: Outcomes and Follow-up From the University Hospital of St. Pölten

NCT07246135 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 700

Last updated 2025-11-24

No results posted yet for this study

Summary

The registry for leadless pacemakers will collect and annually analyze the data of all leadless pacemaker implantations at the University Hospital St. Pölten, including demographic information, indications, procedural details, acute, medium- and long-term complications during follow-up. Due to the partially novel nature of the signals (atrial mechanical sensing markers) and the lack of long-term experience to date, data on these aspects will also be collected and analyzed.

This is a single-center, prospective and retrospective registry that includes all patients receiving a leadless pacing device, as well as all patients who received a leadless pacing device between January 2021 and the start of the registry. All patients undergoing implantation of a leadless pacemaker will be invited to participate in the registry. For patients to be included retrospectively, participation in the registry will be offered at the time of their next routine follow-up visit.

The indication for leadless pacing will be determined by the physician responsible for the patient. Enrollment in the registry will in no case alter or influence the treatment the patient receives. Data collection will take place at the time of implantation and continuously during follow-up over the entire study period. Pacemaker-related data may be obtained either in person or via remote monitoring.

Conditions

  • Pacemaker
  • Leadless Pacemaker
  • Cardiac Pacing, Artificial
  • Registries

Sponsors & Collaborators

  • University Hospital St. Polten

    collaborator OTHER

  • Karl Landsteiner University of Health Sciences

    lead OTHER

Principal Investigators

  • Julia Mascherbauer, MD, Professor · Department of Internal Medicine III, University Hospital of St. Pölten

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-18
Primary Completion
2035-01-31
Completion
2035-01-31

Countries

  • Austria

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 NCT07246135 on ClinicalTrials.gov