Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06774365

CARdiac Imaging and BIomarkers in the Diagnosis of Antibody Mediated Rejection in Heart Transplantation

The goal of this observational study is to systematically assess the presence and distribution of CMR-defined inflammation and fibrosis in clinically stable HT recipients with DSA detected during active screening for AMR surveillance. The main outcome is to study the prevalence of fibrosis, edema and of altered T1 mapping values in patients with DSA and the prevalence of patients with DSA among all the enrolled patients

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Azienda Ospedaliera Universitaria Consorziale Policlinico di Bari, Bari, Italy

Loading trial locations.

About this study

This is a multicentric prospective study with experimental sample collection. Therapy and procedures will be performed according to clinical practice and current guidelines. Caring physicians will be blinded to the results of study specific assays, which will not be used to change standard cynical decision making.

Patients will be enrolled in the study at the time of the DSA assay performed in the context of standard surveillance (yearly monitoring for anti-HLA antibodies is recommended by current guidelines and is part of routine clinical practice). At study entry patients will receive blood sampling to assay dd-cfDNA (centralized laboratory) and T-reg populations (local laboratory). Clinical characteristics, medical history, and results of standard laboratory tests will be collected at baseline.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 18 years
  • Post heart transplantation follow-up between 1 and 15 y
  • Ambulatory clinical stable
  • Left ventricular ejection fraction (LVEF) > 40% (as assessed by complete cardiac ultrasound within 3 months before the enrolment)

Exclusion criteria

  • Unplanned hospitalization for cardiovascular causes in the previous three months
  • Biopsy-proven cellular (2R or greater) or AMR (pAMR> 1 ) in the previous 3 months
  • Any contraindication to CMR
  • Known pregnancy

Treatment and study plan

Primary outcomes

  1. prevalence of fibrosis, edema and of altered T1 mapping values in patients with donor specific antibodies (DSA)

    Time frame: 5 years

    prevalence

  2. prevalence of patients with DSA among all the enrolled patients

    Time frame: 5 years

    prevalence

Secondary outcomes

  1. differences in dd-cfDNA in patients with and without DSA

    Time frame: 5 years

    differences in dd-cfDNA

  2. differences in T-reg subpopulation in patients with and without DSA

    Time frame: 5 years

    differences in T-reg subpopulation

  3. differences in T-reg and dd-cfDNA in patients with and without abnormal CMR

    Time frame: 5 years

    differences in T-reg and dd-cfDNA

  4. change in DSA, biomarkers and CMR findings after vs before AMR treatment

    Time frame: 5 years

    change in DSA

  5. MACE occurrence

    Time frame: 5 years

    MACE occurrence

Study contacts

Contact information is provided by the study sponsor or research team.

Luciano Potena, MD

CONTACT

[email protected]

0512143725

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Collaborators

  • ASST Grande Ospedale Metropolitano Niguarda
  • Azienda Ospedaliera dei Colli
  • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari

Registry information

Acronym: CARIBIAM

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Jan 14, 2025
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.