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Starting soon Observational

European Registry of Acutely Decompensated Pulmonary Arterial Hypertension

NCT06923917 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-12-01
Last updated
2025-11-24

Condition(s) studied

Pulmonary Hypertension

Study summary

Acute decompensation of pulmonary hypertension (PH) is associated with a very unfavorable short-term prognosis. However, the development of circulatory support techniques and the possible use of emergency transplantation in recent years has significantly changed the management of patients with refractory right ventricular failure. Nonetheless, there are significant disparities in the management of these patients depending on the organization of the care pathway, the rules for graft allocation, and access to circulatory support across European countries. Moreover, the implementation of these new therapeutic strategies requires the identification of effective prognostic factors and the development of new monitoring techniques. The objective of this collaborative clinical research project is to study the prognostic implications of acute decompensated right heart failure associated with PAH based on a large-scale European multicenter approach using a prospective analysis of clinical, biological, and echocardiographic data.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Patients with established diagnosis of pulmonary arterial hypertension (group 1) according to the 2022 ESC/ERS guidelines. 2. Worsening of clinical signs of right heart failure in the month prior to hospital admission requiring the use of: * intravenous diuretic therapy for ≥ 2 days * or inotropes * or vasopressors Exclusion Criteria: 1. Patients with non-group 1 pulmonary hypertension 2. Shock due to a cause other than right heart failure 3. Person unable to provide written informed consent (person deprived of liberty by judicial or administrative decision) 4. Person who is the subject of a legal protection measure (tutelage, guardianship, safeguard of justice) 5. Person under psychiatric care 6. Patient's objection to the use of their data

Primary outcome measure(s)

  • 3-months mortality/lung transplantation — 3-months post inclusion
    3-months mortality/lung transplantation

Trial sites (1)

FacilityCityRegionStatus
Assistance Publique hopitaux de Paris Le Kremlin-Bicêtre France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06923917 on ClinicalTrials.gov ↗ ← All trials in France