Skip to main content
OpenTrials
Completed

NCT Number: NCT01616394

Postoperative Troponin in Children With Congenital Heart Disease

The aim of the study is to evaluate the value of postoperative troponin in the prediction of mid term and long term mortality and morbidity in children with congenital heart disease undergoing cardiac surgery.

Completed

Looking for future studies?

Notify Me

Key information

Age range

Up to 10 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Cliniques Universitaires saint Luc

Brussels, 1200, Belgium

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all children with congenital heart disease between 0-10 years admitted for elective or emergency corrective or palliative cardiac surgery

Exclusion criteria

  • parental refusal
  • children older than 10 years

Treatment and study plan

Primary outcomes

  1. mortality

    Time frame: 3 months

Secondary outcomes

  1. morbidity and mortality and length of stay in the PICU and in the hospital

    Time frame: in hospital; 3 months; 6 months

Sponsors and collaborators

Lead sponsor

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Other

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Jun 11, 2012
Registry last updated
Nov 19, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.