Observatory of Pulmonary Arterial Hypertension of Congenital Heart Disease

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02260362

Acronym

ItinerAir

Enrollment

349

Registered

2014-10-09

Start date

2014-10-31

Completion date

2022-07-31

Last updated

2022-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Arterial Hypertension of Congenital Heart Disease

Brief summary

The complex congenital cardiac malformations are a significant number of different diseases, each having specific natural histories. The interface with pulmonary arterial hypertension (HTAP) is high since the physiology of many of these disorders comprises alterations in pulmonary vasculature. This observatory is a cohort of 400 patients enrolled in 3 years, older than one month, having been informed and have agreed to participate in the study and with congenital heart disease other than patent foramen ovale as well as a diagnosis of pulmonary hypertension confirmed by cardiac catheterization. The main objectives of this report are to know * Incidence of congenital heart disease in HTAP France. * Describe the natural history of HTAP in a large population of patients Congenital heart disease in France * The characteristics of HTAP congenital heart disease * Having a cohort study

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

1 Months to No maximum

Healthy volunteers

Inclusion criteria

* The patient has a congenital heart disease other than patent foramen ovale * The diagnosis of pulmonary hypertension was confirmed by cardiac catheterization. Only patients with Eisenmenger syndrome can be included without catheterization. * The catheterization was done after 1 January 2009 * A mean pulmonary artery pressure \> 25 mm Hg * Pulmonary vascular resistances \> 3 piece Wood m2 * Pulmonary capillary pressure available * Consent for inclusion in the study must be signed by parents or legal guardians for minors, by the patient for adults. * The patient he had a surgical procedure or interventional catheterization cardiac catheterization between his diagnosis and inclusion in the observatory? If yes, it can only be included if a new catheterization confirmed the persistence of HTAP at least 6 months after the procedure. * Patient follow-up (at least once a year) in the center for its HTAP associated with congenital heart disease its

Design outcomes

Primary

Measure	Time frame	Description
Incidence HTAP of congenital heart disease in France.	3 years	Number of HTAP of congenital heart disease in France after 3 years of inclusions

Countries

France

Outcome results