NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

Inflammatory Disease Biobank for Immunophenotyping and Cardiovascular Research
Inflammatory Disease Biobank for Immunophenotyping and Cardiovascular Research

NCT07737470

Not Yet RecruitingN/A

Sponsor: Assistance Publique - Hôpitaux de Paris

Conditions: Pericarditis, Tako-TSUBO Cardiomyopathy, Myocarditis, Inflammatory Cardiomyopathies, Lupus

INFLAME-BANK is a French multicenter prospective observational ancillary study of the international EACVI-INFLAME project. It aims to establish a biobank and perform immunophenotyping and proteomic analyses in patients with suspected inflammatory cardiovascular diseases and autoimmune rheumatic diseases (ICARDs). The primary objective is to identify immune biomarkers associated with cardiovascular prognosis and develop disease-specific prognostic scores to predict 1-year major adverse cardiovascular events (MACE). Secondary objectives include evaluating the diagnostic and prognostic value of immunoproteomic biomarkers, assessing the role of photon-counting CT (PCCT) imaging, and investigating immune signatures associated with genetic variants in acute myocarditis. The study plans to enroll 300 patients from French centers participating in EACVI-INFLAME. Blood samples will be collected during routine clinical care at inclusion, with optional follow-up sampling at 12 months and optional PCCT imaging and genetic analyses depending on each center's participation. Patients will be followed for 12 months to monitor cardiovascular outcomes. The expected impact is to improve understanding of the immune mechanisms underlying ICARDs, facilitate earlier diagnosis and risk stratification, identify new therapeutic targets, and ultimately support more personalized management of patients with inflammatory cardiovascular diseases.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* Patient enrolled in EACVI-INFLAME study
* The patient consents

Exclusion Criteria:

* Patients with a history of heart transplant
* Patient unable to provide informed consent
* Patient under complete or limited guardianship
* Patient affected by pre-existing immunodeficiency, including HIV (not including immunosuppressive treatment)