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Clinical Trials in France / NCT07157670
Recruiting Observational

Cardiovascular Complications in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation.

NCT07157670 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-12-25
Last updated
2026-09-25

Condition(s) studied

CardiotoxicityDPP3HSCTAllogeneic Hematopoietic Stem Cell TransplantationACS - Acute Coronary SyndromeCardiac DysfunctionArrythmia, CardiacPulmonary HypertensionMachine Learning

Study summary

Allogeneic hematopoietic stem cell transplantation (HSCT) represents a major therapeutic strategy for malignant hematologic diseases, with the number of procedures steadily increasing in France each year. Conditioning and maintenance regimens carry a risk of both short- and long-term cardiotoxicity, leading to serious cardiovascular events including acute coronary syndrome (ACS), cardiac dysfunction, arrhythmias, pulmonary hypertension, and pericardial effusion. The pathophysiology of cardiotoxicity in HSCT patients remains poorly understood.

It is therefore crucial to investigate underlying mechanisms and identify predictive factors of cardiotoxicity in order to provide appropriate cardiological follow-up and management. Current European Society of Cardiology guidelines recommend routine monitoring of HSCT patients with echocardiography and cardiac biomarkers (NT-proBNP, troponin), although these recommendations are based on small-scale studies. The cardiodepressor factor DPP3 has shown promising results in cardio-oncology, with a causal role in anthracycline-induced cardiac dysfunction. Its role in HSCT-related cardiotoxicity requires further evaluation.

This multicenter study of HSCT recipients will be a valuable resource, enabling a better understanding of the pathophysiology of cardiotoxicity and prognosis. It will highlight imaging (echocardiography, calcium score, supra-aortic Doppler), electrocardiographic, and biological markers (including DPP3) associated with prognosis.

Eligibility

Sex
ALL
Min age
15 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 15 years * Informed about the study and without objection to participation (or with consent from legal guardians) * Undergoing allogeneic HSCT Exclusion Criteria: * Patient not followed up at the participating center * Pregnant or breastfeeding women * Patient not affiliated with social security * Patient under guardianship, curatorship, or legal protection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Saint Louis Hospital Paris France Recruiting

More Assistance Publique - Hôpitaux de Paris trials in France

Other trials for the same condition

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 NCT07157670 on ClinicalTrials.gov ↗ ← All trials in France