Menu
Enrolling by invitation NCT04926792

Taiwan Registry for Leadless Pacemaker

— Observational Sick Sinus Syndrome Atrioventricular Block

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Leadless Pacemaker.
Who it may be relevant to
Registry conditions: Sick Sinus Syndrome, Atrioventricular Block. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Taiwan Registry for Leadless Pacemaker is a nationwide registry for leadless pacemaker performance in Taiwan.

Detailed description

The purpose of this registry is to investigate the safety and efficiency performance of the leadless pacemakers in Taiwan. The registry will collect all the information about the patient selection, implantation procedure, and follow up parameters of the leadless pacemakers to evaluate the real-world benefit specifically in Taiwan population.

Interventions

  • Device Leadless Pacemaker
    Leadless pacemaker implantation

Primary outcome measures

  • Acute complication [Time frame: On the 1 day of implant procedure]
  • Subacute complication [Time frame: within 3 month after implant procedure]
  • Leadless Pacemaker performance [Time frame: aroung 12 months after implant proceure]
Secondary outcome measures (1)
  • Successful implant [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • The patients who had successfully received leadless pacemaker implantation
  • The patients who attempt to receive leadless pacemaker implantation

Exclusion criteria

N/A

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Taiwan · 1 center
  • National Taiwan University Hospital — Taipei

Identifiers

NCT: NCT04926792 · 202103105RINB

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗