Registry for implantable cardiac devices

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This registry focuses on the implantation of cardiac devices such as pacemakers and implantable cardioverter-defibrillators, which are standard procedures in managing cardiac arrhythmias. It aims to evaluate the efficacy and safety of these devices while identifying clinical and procedural factors that may influence patient outcomes. By monitoring advancements in device technology and patient care, the registry seeks to enhance the overall management of patients with conditions like syncope, bradycardia, and sudden cardiac death.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. pre-operative clinical history taking
2. pre-operative functional investigations (cardiac echo, electrocardiograms)
3. pre-operative laboratory data evaluation (kidney function, liver function, biomarkers, thyroid hormone, CBC)

Exclusion Criteria:

１. no written informed consent

Where it's running

• Division of Cardiology, Pulmonary Disease and Vascular Medicine
  Düsseldorf, Germany Recruiting

Study contacts

• Principal investigator: Hisaki Makimoto, MD — Division of Cardiology, Pulmonary Disease and Vascular Medicine
• Study coordinator: Hisaki Makimoto, MD
• Phone: +492118118800

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.