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OpenTrials
Completed

NCT Number: NCT03913520

Outcome of Patients With Congenital Heart Disease

Advanced surgical and medical healthcare systems have resulted in an increased prevalence of children and adults with congenital heart disease in Western countries. These patients often necessitate non-cardiac interventions. Previous studies have demonstrated that these patients are at increased risk of morbidity and mortality when presenting for non-cardiac interventions. The aim of this study is to know the prevalence of patients with congenital heart disease presenting for non-cardiac interventions in a tertiary hospital and to determine their outcome.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cliniques Universitaires Saint Luc

Brussels, 1200, Belgium

About this study

Previous studies have shown that children and adults presenting with congenital heart disease are at increased risk of morbidity and mortality after non-cardiac interventions. This risk depends on the type of pathology, the age of the patient and the experience of the physicians in charge of these patients.

We sought to determine the prevalence of children and adults with congenital heart disease presenting for non-cardiac interventions and to investigate their outcome.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All children and adults with congenital heart disease

Exclusion criteria

  • Parental or patient refusal
  • Patients presenting for cardiac interventions

Treatment and study plan

Outcome research

Other

patients will undergo an evaluation of their outcome at 30 days postoperatively

Primary outcomes

  1. The prevalence of patients with congenital heart disease presenting for non-cardiac interventions in a single-centre tertiary hospital

    Time frame: Intraoperative

    To analyze the exact number of children and adults with congenital heart disease presenting for non-cardiac interventions in a tertiary hospital

Secondary outcomes

  1. To analyze morbidity after non-cardiac interventions in patients with congenital heart disease

    Time frame: 30 days

    Morbidity outcome after non-cardiac interventions

  2. To analyze mortality after non-cardiac interventions in patients with congenital heart disease

    Time frame: 30 days

    Mortality outcome after non-cardiac interventions

Sponsors and collaborators

Lead sponsor

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Other

Registry information

Official study title

Postoperative Outcome of Patients With Congenital Heart Disease Presenting for Non-cardiac Interventions

Acronym: OUTCARDIOP

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Apr 12, 2019
Registry last updated
Oct 22, 2020

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.

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