ClinicalTrials.gov record NCT06813443
Characterization of Patients With Cardiomyopathy to Identify Critical Patients Candidates for Cardiac Transplantation
Clinical, Instrumental, and Molecular (Circulating and Tissue microRNAs) Characterization of Patients With Cardiomyopathy to Identify Critical Patients With Severe Organ Failure to be Candidates for Cardiac Transplantation
AI summaryWhat this study is about, in plain languageShow ▾Hide ▴
AI-written from the registry record, not the study's own wording. May contain errors or omissions. Check the registry text on this page and the original record ↗ before acting on it.
This observational cohort study enrolls people aged 12 and older with various cardiomyopathies. It combines retrospective chart data and prospective follow-up across multiple centers to collect clinical, imaging, pathology, genetic, and molecular data. A subgroup will provide blood and, when clinically performed, heart tissue for microRNA and spatial transcriptomics analyses.
What it is studying. The study looks for diagnostic and prognostic markers (including microRNAs and spatial transcriptomics) that, together with clinical and imaging data, can identify disease subtypes and patients who may progress to heart failure or require transplant. It also evaluates how combinations of clinical, instrumental, histological, and molecular variables perform for risk stratification.
What the researchers hope to learn. Scientific goals: identify new diagnostic and prognostic biomarkers (plasma and tissue microRNAs and spatial transcriptomics); develop and test risk‑stratification tools to identify patients with advanced disease or who may need transplantation; build diagnostic models to help distinguish AL versus TTR cardiac amyloidosis when integrated with clinical and imaging data.
What this study is about
The study's own summary, as published on ClinicalTrials.gov. Underlined terms have a short explanation.
The study aims to identify new diagnostic and prognostic markers for CMP that can help predict disease progression. In particular, the study will focus on microRNAs (miRNAs) and spatial transcriptomics, which are emerging techniques that may provide insights into the underlying disease mechanisms. By understanding these markers, the investigators hope to improve the way the investigators diagnose and manage CMP, particularly in terms of predicting progression to heart failure or heart transplantation. The study will evaluate patients with hypertrophic cardiomyopathy (e.g., sarcomeric forms, Anderson-Fabry disease, AL, and TTR cardiac amyloidosis), dilated cardiomyopathy and arrhythmogenic cardiomyopathy. These patients will undergo clinical evaluations, including ECG, echocardiograms, CMR, biopsy analysis, and genetic testing, as well as molecular studies such as transcriptomics and miRNA analysis. This comprehensive approach aims to identify potential new biomarkers for diagnosing and predicting the disease course.
Eligibility
The criteria exactly as listed on ClinicalTrials.gov. Only the study team can say whether they apply to you.
Inclusion criteria
- Patients diagnosed with CMP according to current international guidelines
- Age ≥ 12 years at the time of diagnosis
- Obtaining informed consent from the patient and the parent or legal guardian (in the case of patients aged < 18 years)
Exclusion criteria
- none
Study description and what participation involves
The study's detailed description, as published on ClinicalTrials.gov.
Show the detailed description from the registry
This is a non-pharmacological, national multicenter cohort study with both retrospective and prospective components. For the prospective study, patients with CMP will be consecutively enrolled from the outpatient or inpatient settings of the IRCCS Azienda Ospedaliero-Universitaria di Bologna (coordinating center), Azienda Ospedaliero-Universitaria Careggi di Firenze, and the Department of Cardiothoracic and Vascular Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome. Enrollment will begin upon receipt of favorable opinions from the respective Ethics Committees and general management approvals at each center until the planned sample size is reached. For the retrospective study, all patients managed at the aforementioned centers prior to obtaining Ethics Committee approval and general management clearance will be included. The structured collection of the data necessary for the evaluation of the objectives will be carried out by creating a specific electronic database in which retrospective data will be collected starting from January 1, 1990, and for the prospective observation period from the moment of ethical committee approval and receipt of the clearance from the general director until December 31, 2027. The electronic archive may be used to obtain or confirm new scientific evidence in the field of CMP, particularly with reference to diagnosis, prognosis, and therapy. The electronic archive will be compiled through the consultation of the clinical records (outpatient or hospitalization), from which data regarding demographics, remote and recent medical history, family history, any genetic investigations, instrumental tests, information about symptoms at onset, and therapy will be collected. Aside from the analysis of miRNAs on tissues, which will be carried out for the study and will not in any way affect the patients' diagnostic-therapeutic path, all instrumental exams and therapies that patients will undergo are part of standard clinical practice. Any genetic investigations that patients may undergo are part of the regular care pathway and will be performed when clinically indicated, or if a precise etiological diagnosis is necessary, with consequent therapeutic implications, in the differential diagnosis between various forms of CMP, and when, in the context of familial forms, it may be useful for family screening. Patients will be enrolled during hospitalization or at the outpatient visit. After obtaining informed consent, patients will be evaluated based on clinical needs. There is no minimum duration for following the patient. In a subgroup of patients enrolled in the prospective study, additional molecular evaluations will be carried out on plasma and cardiac tissue. The blood sample-taken as per clinical practice-will be processed within 4 hours through centrifugation. After isolation, the plasma will be divided into aliquots of 500 µL and stored at -80°C. In the subpopulation of the study undergoing endomyocardial biopsy (diagnostic) or cardiac surgery (e.g., myectomy, valve replacement, etc.), according to the standard-of-care, fresh cardiac tissue will be collected. The cardiac tissue (taken during endomyocardial biopsy/cardiac surgery performed according to clinical practice) will be partially immersed in formalin and sent, as per normal procedure, to pathology where it will be processed for paraffin embedding, and a small fragment will be frozen and immediately embedded in OCT (optimal cutting temperature) and stored at -80°C. RNA will then be extracted and analyzed using NGS (next-generation sequencing) of small RNA, ddPCR (droplet digital Polymerase Chain Reaction), and spatial transcriptomics.
AI summaryWhat participation may involve, in plain languageShow ▾Hide ▴
AI-written from the registry record, not the study's own wording. May contain errors or omissions. Check the registry text on this page and the original record ↗ before acting on it.
For retrospective participants the study uses existing medical records. Prospective participants undergo routine clinical evaluations (for example ECG, echocardiogram, cardiac MRI as clinically indicated), and genetic testing when clinically needed. Blood samples will be drawn and processed for plasma microRNA analysis and stored; cardiac tissue will only be collected if an endomyocardial biopsy or cardiac surgery is performed as part of standard care, and those samples will be frozen for molecular tests (including miRNA and spatial transcriptomics, NGS and ddPCR). There is no minimum follow-up duration; participation requires informed consent (and parental/legal-guardian consent for minors).
How the study is structured. Non‑drug, multicenter observational cohort with both retrospective and prospective parts. Retrospective data are collected from clinical records (from 1990 onward) and prospective patients are followed and entered into an electronic database; standard clinical tests (ECG, echocardiogram, cardiac MRI, biopsies, genetic testing) are used. In a prospective subgroup, blood samples and heart tissue obtained during clinically indicated biopsy or surgery are stored and analyzed for microRNA and spatial transcriptomics.
Questions you could ask
These questions are suggestions for a conversation with the study team or your own clinician, not advice.
- This is an observational study, so the study itself gives no treatment. What would taking part involve for me, and would it change my usual care?
- The listed sites are in Italy. Is any of them reachable for me, and does the study help with travel?
- Which of the eligibility criteria would need to be checked with tests before I could join?
More on Fabry disease
This trial is also listed on this site under ATTRv amyloidosis and wild-type ATTR amyloidosis.
Important dates
- Study start
- Feb 13, 2023
- Primary completion
- Jun 30, 2027 (estimated)
- Study completion
- Dec 14, 2027 (estimated)
- Target enrollment
- 700 participants (estimated)
- Last updated on registry
- Feb 7, 2025
- Data verified
- Oct 10, 2026
Sponsor and research team
The lead sponsor funds and oversees the trial. A pharmaceutical or biotech company sponsor typically means the study is testing that company's drug or device; a hospital, university, or government agency usually indicates investigator-initiated or publicly funded research.
- Lead sponsor
- IRCCS Azienda Ospedaliero-Universitaria di Bologna
Central study contact
If you're interested in participating, the central contact can answer general questions about the study — including eligibility requirements and how to find a recruiting site near you. Actual eligibility is determined by the site's medical team.
- Elena Biagini, MD, PhD 📞 +39051214483 ✉ elena.biagini@aosp.bo.it
- Silvia Palmieri, M. Sc. 📞 +39051214483 ✉ silvia.palmieri@aosp.bo.it
Participating sites (3)
- IRCCS Azienda Ospedaliero-Universitaria di BolognaRecruiting
Bologna, Emilia-Romagna/Bologna, 40138 · Italy
- Elena Biagini, MD, PhD · +39 051 214 4483 · elena.biagini@aosp.it
- Silvia Palmieri, M.Sc. · +39 051 214 4483 · silvia.palmieri@aosp.bo.it
- Dipartimento di Scienze Toraciche Cardiovascolari, Fondazione Policlinico Universitario A. Gemelli IRCSS di RomaNot Yet Recruiting
Roma, Lazio/Roma, 00161 · Italy
- Francesca Graziani, MD · +39 0630154639 · francesca.graziani@policlinicogemelli.it
- Azienda Ospedaliero-Universitaria Careggi di FirenzeNot Yet Recruiting
Florence, Toscana/Firenze, 50134 · Italy
- Iacopo Olivotto, MD · +39 3333314844 · iacopo.olivotto@gmail.com
Terms used on this page · explanations by MedicalUpdates.ai
- ECG
- A recording of the heart's electrical activity. QTc is one measurement from it; some drugs are avoided if it is prolonged.
- biopsy
- Removal of a small piece of tissue so it can be examined under a microscope. 'Biopsy-proven' or 'histologically confirmed' means the diagnosis was confirmed by examining tissue under a microscope.
- biomarkers
- Something measurable in the body, such as a blood test result or an imaging finding, that indicates how a condition or treatment is behaving.
- informed consent
- The process of explaining a study, including its risks and what participation involves, so that a person can decide freely whether to take part. Consent is usually documented in writing, and a participant can choose to leave the study later.
- legal guardian
- A person who is legally allowed to make decisions, including consent to research, on behalf of someone who cannot consent for themselves.
- Inclusion Criteria
- The conditions a person must meet to be considered for the study, for example a confirmed diagnosis, an age range or a test result.
- Exclusion Criteria
- The conditions that rule a person out even if they meet the inclusion criteria, for example other illnesses, certain medicines or pregnancy.
- cohort study
- A group of people who share a characteristic, such as a diagnosis, and are studied together. 'Prospective' means they are followed forward from enrolment; 'retrospective' means existing records are reviewed.
- Enrollment
- The number of participants a study plans to include, or has included. 'Estimated' means the planned number; 'actual' means the number who joined.
The study record on this page is reproduced from ClinicalTrials.gov, a database of the U.S. National Library of Medicine, where it was submitted by the study sponsor. MedicalUpdates.ai does not own this content, is not affiliated with or endorsed by ClinicalTrials.gov, NIH, or the U.S. Government, and does not verify the record. Plain-language notes, the glossary and the questions above are added by this site; text in the boxes marked "AI summary" was written by an AI model and may contain errors. Registry records change over time. Check the original record for the current version and discuss eligibility or participation with a qualified healthcare professional.
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