Essen Amyloidosis Registry
Recruiting now
Conditions studied: Amyloidosis; Systemic, Amyloidosis Cardiac
In brief
The Essen Amyloidosis Registry (EAR) is a prospective, observational registry designed to collect comprehensive clinical data on patients diagnosed with systemic amyloidosis. The registry aims to improve the understanding of disease progression, diagnostic pathways, and treatment outcomes. The registry is hosted at the University Hospital Essen and follows patients longitudinally. Inclusion is open to all patients with suspected or confirmed amyloidosis who provide informed consent.
Key facts
- Study ID
- NCT06887283
- Run by
- University Hospital, Essen
- People needed
- 400
- Starts
- 2024-05-08
- Expected to finish
- 2029-07-01
- Last updated by the study team
- 2025-08-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Suspected or confirmed amyloidosis (any)
- Written informed consent to participate in the study
- Age 18 years and above
You may not qualify if…
- Age < 18 years
- Lack of written informed consent
Where it is running
- University Hospital Essen — Essen, North Rhine-Westphalia, Germany (enrolling)
Full record on ClinicalTrials.gov
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