Actively Recruiting

Age: 0 - 18Years
All Genders
NCT05373498

Resuscitation Registry in CHD

Led by Leipzig Heart Science gGmbH · Updated on 2025-01-16

400

Participants Needed

3

Research Sites

541 weeks

Total Duration

On this page

Sponsors

L

Leipzig Heart Science gGmbH

Lead Sponsor

H

Heart Center Leipzig - University Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Children with congenital heart defects are far more likely to suffer a cardiovascular arrest and be in the need of cardiopulmonary resuscitation than healthy children or those with diseases of other organ systems, especially after cardiothoracic surgery. Due to a lack of data, the exact number of resuscitations in this patient cohort, as well as the morbidity and mortality, is unknown. This study aims to register all cardiovascular arrests in pediatric patients with congenital heart disease and study the mortality and morbidity with a special focus on the neurodevelopmental outcome.

CONDITIONS

Official Title

Resuscitation Registry in CHD

Who Can Participate

Age: 0 - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children under 18 years with congenital heart defects, congenital heart arrhythmias, familial cardiomyopathies, or inflammatory heart diseases
  • Cardiac arrest requiring chest compressions for at least 2 minutes in hospital or upon hospital arrival
  • Informed consent provided by parents or legal representatives
Not Eligible

You will not qualify if you...

  • Lack of or withdrawal of informed consent by parents or legal representatives
  • Presence of a do-not-resuscitate (DNR) order

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Herzzentrum Leipzig

Leipzig, Saxony, Germany, 04289

Actively Recruiting

2

Deutsches Herzzentrum Berlin

Berlin, Germany, 13353

Not Yet Recruiting

3

Universitätsklinikum Bonn (AöR)

Bonn, Germany, 53127

Not Yet Recruiting

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Research Team

F

Franziska Markel, Dr. med.

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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