Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT03360227

Registry of Device Implantation

Led by Klinik für Kardiologie, Pneumologie und Angiologie · Updated on 2020-02-07

2000

Participants Needed

1

Research Sites

1039 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The implantable device therapy for cardiac arrhythmias has been an established therapy, and one of the common standard procedures in cardiac clinical practice. Pacemakers, implantable cardioverter-defibrillators, and cardiac resynchronization therapy have been developed since 1960s, and the technologies in this field are still progressively developing. Not only these "traditional" implantable devices, there are multiple new devices for cardiac diseases, such as implantable loop recorder, vagal nerve stimulator and barostimulator. The aim of this registry is to demonstrate the efficacy and the safety of standard device implantation procedures and to evaluate/ identify specific factors, including clinical characteristics, laboratory data and procedural data, which predict the prognosis/complication of the patients. These identification will result in further improvement of patients' care.

CONDITIONS

Official Title

Registry of Device Implantation

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pre-operative clinical history taken
  • Pre-operative functional investigations including cardiac echocardiograms and electrocardiograms
  • Pre-operative laboratory evaluations including kidney function, liver function, biomarkers, thyroid hormone, and complete blood count
Not Eligible

You will not qualify if you...

  • No written informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Division of Cardiology, Pulmonary Disease and Vascular Medicine

Düsseldorf, Germany, 40225

Actively Recruiting

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Research Team

H

Hisaki Makimoto, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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