Clinical Trials in Spain / NCT06205953
Recruiting
Observational
A EUropean REgistry and Sample Sharing networK to Promote the Diagnosis and Management of Light Chain Amyloidosis (EUREKA)
NCT06205953 · tracked via the Priya Life Science Spain tracker
Condition(s) studied
AL Amyloidosis
Study summary
A prospective patients' registry collecting all new cases of AL amyloidosis evaluated at referral Centers from across Europe and a sample sharing network will be created to study mechanisms of the disease through the use of advanced molecular technologies and big data analysis tools.
Eligibility
Inclusion Criteria:
* diagnosis of systemic AL amyloidosis;
* treatment-naïve;
* age ≥18 years;
* ability to understand and willingness to sign an informed consent;
* planned follow-up at participating center.
Exclusion Criteria:
* non-AL amyloidosis;
* previous treatment for AL amyloidosis.
Primary outcome measure(s)
- Mortality at 24 months by stage — 24 months from diagnosis
Mortality at 24 months by stage will be evaluated
Trial sites (6)
| Facility | City | Region | Status |
|---|---|---|---|
| Medical Department, Amyloidosis Center, University Hospital, Im Neuenheimer Feld 672 | Heidelberg | Germany | Recruiting |
| Fondazione IRCCS Policlinico San Matteo, Pavia, Viale Golgi 19, 27100 | Pavia | Italy | Recruiting |
| UMC Utrecht, dept Hematology, Amyloid Expertise Center, Utrecht, Heidelberglaan | Utrecht | Netherlands | Recruiting |
| Instituto de Investigación Sanitaria de Navarra (IdiSNA) C. de Irunlarrea, 3, 31008 Pamplona, Navarra | Pamplona | Spain | Recruiting |
| University of Applied Sciences and Arts Northwestern Switzerland, Institute of Medical Engineering and Medical Informatics | Muttenz | Switzerland | Active Not Recruiting |
| Universidad de la Republica Hospital de Clinicas "Dr Manuel Quintela" | Montevideo | Uruguay | Recruiting |
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06205953 on ClinicalTrials.gov ↗ ← All trials in Spain