Understanding patients with transthyretin cardiac amyloidosis
Official title: Description of a Retrospective Cohort of Patients With Transthyretin Cardiac Amyloidosis (ATTR-CA) in Internal Medicine
Run by University Hospital, Strasbourg, France · NCT06907836 · Data updated 2026-11-12
This study looks at patients with transthyretin cardiac amyloidosis to learn more about how the disease affects their hearts and overall health over time.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | University Hospital, Strasbourg, France Academic / other |
| Locations | 1 site (Strasbourg) |
| Status | Recruiting |
| Started | April 22, 2024 |
| Main results expected | December 22, 2025 |
| Study ends | December 22, 2025 |
| Registry record updated | April 2, 2025 |
| Trial ID | NCT06907836 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 and older who have been diagnosed with transthyretin amyloidosis following hospitalization in internal medicine at the University Hospital of Strasbourg.
✕Probably not a fit
Patients with types of amyloidosis other than ATTR or those who have opted out of data reuse for research will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to characterize a cohort of patients diagnosed with transthyretin cardiac amyloidosis (ATTR-CA) at the University Hospital in Strasbourg, France. It focuses on the prevalence and natural history of the disease, particularly in relation to heart failure with preserved ejection fraction. The study will analyze patient data collected from hospitalizations in internal medicine over a ten-year period, from 2013 to 2023, to better understand the progression and outcomes of ATTR-CA. By examining this cohort, the study seeks to shed light on the underdiagnosed nature of the condition and its impact on patient survival.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of ATTR-CA, leading to improved diagnosis and management strategies for patients.
How similar studies have gone: While there is limited data on similar observational studies specifically focusing on ATTR-CA, the increasing recognition of the condition suggests that this approach could yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Sujet majeur (≥18 ans) * Diagnostic d'amylose à TTR suite à une hospitalisation en médecine interne aux HUS entre 01/01/2013 au 31/12/2023. Exclusion Criteria: * Subject (and/or their legal representative, if applicable) who has expressed their opposition to the reuse of their data for scientific research purposes. * Type of amyloidosis other than ATTR after review of the medical record (immunological assessment, imaging assessment, expert report).
Where it's running
-
Service de Médecine Interne - CHU de Strasbourg - France
Strasbourg, France Recruiting
Study contacts
- Study coordinator: Emmanuel ANDRES, MD, PhD
- Email: emmanuel.andres@chru-strasbourg.fr
- Phone: 33 3 88 12 71 33
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Liver and Coagulation Markers in ATTR Cardiac Amyloidosis
This study tests liver function and blood-clotting markers in people with ATTR-CA to see if they reflect disease severity and progression.
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Cardiac Amyloidosis: See if Intracardiac Thrombi are Common on CT
This study tests whether a contrast-enhanced cardiac CT can reliably detect intracardiac thrombi in adults with cardiac amyloidosis.
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Higher pacemaker rate for people with cardiac amyloidosis
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We'll test whether a [64Cu]FBP8 PET/MR scan can find blood clots inside the heart of people with cardiac amyloidosis who have atrial fibrillation or atrial flutter.
-
Chest pain screening for hidden cardiac amyloidosis
We will test whether men over 65 who have chest pain but no coronary artery disease might have hidden cardiac amyloidosis using blood and urine tests, ECG and echocardiography, bone scintigraphy, and sometimes a heart biopsy.
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This project tests whether advanced cardiac MRI techniques can help diagnose and predict future risk for people with rare heart muscle diseases like Danon, Fabry, cardiac amyloidosis, Noonan syndrome, and cardiac sarcoidosis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.