AzTrials
AzTrials

MyocarditisEACVI-INFLAMENCT07077304

EACVI Study on Multimodality Cardiovascular Imaging of Inflammatory Cardiovascular Diseases

An observational study of Myocarditis and ANCA Associated Vasculitis, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

Search all trials

Trial summary

Inflammatory Cardiovascular Diseases and Autoimmune Rheumatic Diseases (ICARDs) encompass cardiovascular involvement in connective tissue diseases, vasculitis, and primary inflammatory cardiac processes affecting all layers of the heart. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
observational study
How many people
5,000 participants
Where
1 siteFrance
Study dates
19 Nov 2025to 30 Oct 2028
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: all patients with a suspicion of cardiovascular involvement due to a suspected or previously diagnosed ICARD referred for a CMR and/or nuclear imaging exam.

Who may be able to join

  • Age ≥ 18 years
  • Ability to provide informed non-opposition
  • Referred for a CMR and/or nuclear imaging exam
  • AND a suspicion of one of the following ICARDs :
  • Suspected Myocarditis (acute or chronic, and whatever the aetiologies)
  • Suspected Myocardial Infarction with Non-Obstructive Coronary Arteries (MINOCA)
Show all 20Show fewer
  • Suspected Tako-Tsubo
  • Suspected Pericarditis (acute or chronic, and whatever the aetiologies)
  • Suspected Connective tissue disease with cardiovascular involvement:
  • Systemic sclerosis
  • Systemic lupus erythematosus
  • Antiphospholipid syndrome
  • Idiopathic inflammatory myopathies
  • Rheumatoid arthritis, spondylarthritis
  • Suspected Vasculitis with cardiovascular involvement:
  • Small-vessel vasculitis (ANCA…)
  • Large vessel vasculitis (Behcet disease, Takayasu…)
  • Suspected Inflammatory disease with cardiovascular involvement:
  • Sarcoidosis
  • Still disease

Who cannot join

  • Inability to provide non-opposition
  • History of heart transplant

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • Assistance Publique Hôpitaux de Paris, Paris, île de France 75010

    Paris

    Théo PEZEL, 668722489 ext. +33, theo.pezel@aphp.fr

    Recruiting

Other trials in France

About this study

Inflammatory Cardiovascular Diseases and Autoimmune Rheumatic Diseases (ICARDs) encompass cardiovascular involvement in connective tissue diseases, vasculitis, and primary inflammatory cardiac processes affecting all layers of the heart. ICARDs are associated with increased cardiovascular morbidity and mortality, independently of traditional risk factors, via multiple pathophysiological mechanisms.

Diagnosis and prognosis are challenged by the heterogeneity of clinical presentations. Multimodality cardiovascular imaging - including cardiovascular magnetic resonance (CMR), transthoracic echocardiography, and positron emission tomography (PET) - plays a central role in detecting and characterizing inflammatory involvement, and may offer prognostic insights.

Given the limited data on the diagnostic and prognostic utility of these imaging modalities in ICARDs, the EACVI-INFLAME study aims to assess the prevalence of confirmed cardiovascular involvement in patients with suspected or established ICARDs undergoing CMR and/or cardiac PET in a multicentric international cohort.

Read the detailed description

Inflammatory Cardiovascular Diseases and Autoimmune Rheumatic diseases (ICARDs) encompass the cardiovascular manifestations of connective tissue diseases and vasculitis, along with primary inflammation affecting all layers of the heart - such as myocarditis, pericarditis and Tako-Tsubo. ICARDs can result in a vast array of clinical cardiovascular manifestations, including coronary artery disease, acute heart failure, ventricular and supra-ventricular arrhythmia. Autoimmune rheumatic disease have been identified as independent risk factors of major cardiovascular events, even after adjusting for traditional cardiovascular risk factors, and accumulated evidence shows increased cardiovascular morbidity and mortality in ICARDs compared to the general population.

Various pathophysiological mechanisms have been proposed to explain the increased risk of cardiovascular events. Suspected mechanisms include prolonged systemic inflammation, accelerated atherosclerosis, autoantibody and immune complex formation, as well as an increase in sympathetic tone which may contribute to heart failure and arrhythmia. Cardiovascular involvement in patients with ICARDs represents a diagnostic challenge due to the heterogeneity in their clinical presentation, and establishing prognosis following cardiovascular involvement is equally difficult. Multimodality cardiovascular imaging, including cardiovascular magnetic resonance (CMR), transthoracic echocardiography and positron emission tomography (PET) nuclear imaging have emerged as useful diagnostic tools to help differentiate inflammatory diseases among themselves and from other diseases, and identify prognostic markers.

Multimodality cardiovascular imaging has the potential to play a major role in assessing the extent of cardiovascular involvement of both primary inflammatory cardiomyopathies and autoimmune rheumatic diseases, by allowing for an early and more accurate diagnosis, phenotypic classification and monitoring. The additive value of cardiovascular imaging, notably MRI, cardiac PET scan, and multimodality imaging in connective tissue disease and vasculitis remains unclear and has been mentioned as a research topic of interest. Moreover, this study will help acquire data on drug tapering, treatment modalities adapted to different etiologies, as well as data on ICARDs unresponsive to treatment. A thorough assessment of the current practices, diagnostic and prognostic value of multimodality imaging in the context of ICARDs has the potential to help shape future guidelines for early assessment of cardiovascular involvement in ICARDs, and potentially change treatment algorithms.

The establishment of this study is particularly pertinent with the forthcoming ESC guidelines on the management of inflammatory cardiomyopathies, as it will provide real-life data on the application of these guidelines. Due to the lack of evidence in the literature on the topic of the diagnostic and prognostic value of multimodality imaging in the context of ICARDs, this "EACVI-INFLAME" international study will aim to determine the proportion of patients with confirmed cardiovascular involvement in patients with suspected or established ICARDs undergoing CMR and/or cardiac PET in a multicentric international cohort.

Being tested
observational study
Keywords
Cardiovascular disease, Auto-immune disease, Auto-inflammatory disease, Rheumatic disease, CMR, PET, multimodality imaging, ICARD
Medical subject headings
Myocarditis, Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis, Pericarditis, Scleroderma, Systemic, Lupus Erythematosus, Systemic, Myositis, Arthritis, Rheumatoid, Spondylarthritis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • observational studyOther

    observational study

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of patients with confirmed cardiovascular involvement among consecutive patients with a suspicion of cardiovascular involvement due to a suspected or known ICARD referred for CMR and/or nuclear imaging exam.

    To assess the proportion of patients with confirmed cardiovascular involvement among consecutive patients with suspected or known ICARD referred for CMR and/or nuclear imaging exam in a multicentre international and prospective study.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

Secondary outcomes (8)
  1. Baseline characteristics

    Epidemiologic distribution of clinical, biological and cardiovascular imaging characteristics at baseline.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  2. Proportion of patients presenting with the clinical composite outcome at 1year follow-up

    Proportion of patients presenting with the clinical composite outcome at 1year follow-up defined as the proportion of patients presenting with:

    • Cardiovascular mortality and/or
    • Hospitalization for heart failure (HF) and/or
    • Myocardial infarction and/or
    • Incident atrial fibrillation and/or
    • Stroke and/or
    • Recurrence of ICARD

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  3. Proportion of patients with all-cause mortality at 1-year follow-up.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  4. Proportion of patients with cardiovascular mortality at 1-year follow-up.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  5. Proportion of patients hospitalized for heart failure at 1-year follow-up.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  6. Proportion of patients hospitalized for an acute episode of ICARD at 1-year follow-up.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  7. Proportion of patients achieving the remission of ICARD at 1-year follow-up.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

  8. Proportion of participants for whom cardiac imaging led to a guideline-concordant diagnosis, according to the cardio-rheumatology team, and specific to each ICARD category.

    Measured: At each diagnostic assessment point, up to study completion, an average of 1 year.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2025
  2. Study start19 Nov 2025
  3. Primary completion31 Aug 2027 (estimated)
  4. Study completion30 Oct 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
5,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07077304
Sponsor's protocol ID
AP-HP250504
Acronym
EACVI-INFLAME
Status last verified
May 2026
First submitted
16 May 2025
Last updated
5 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in