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NCT04839003Recruiting

A Registry of AL Amyloidosis (ReAL)

A Registry to Investigate Real-world Natural History, Impact of Therapies and Patterns of Progression of AL Amyloidosis (ReAL)

Source: ClinicalTrials.gov · Last updated 16 Apr 2026

Brief summary (registry, in English)

The purpose of this protocol is to generate a large registry of patients with AL amyloidosis.

Status (registry)
Recruiting
Study type
Observational
Enrollment
5000 (estimated)
First submitted
22 Mar 2021
Start date
27 Feb 2020
Primary completion date
31 May 2027
Lead sponsor
Fondazione IRCCS Policlinico San Matteo di Pavia
Diseases
Amyloidosis
NCT number
NCT04839003

What you commit to

  • Study type: Observational
  • Planned participants: 5000
  • From 27 Feb 2020 to the primary completion date, 31 May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • previous treatment for AL amyloidosis.

Other

  • non-AL amyloidosis;

Who the study is looking for

  • diagnosis of systemic AL amyloidosis;
  • treatment-naïve (pre-treatment data collected at participating center available for retrospective part);
  • age ≥18 years;
  • ability to understand and willingness to sign an informed consent (patients who already sign informed consent for clinical data to be used in retrospective analyses will be accepted);
  • planned (or ongoing) follow-up at participating center.

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fondazione IRCCS Policlinico San Matteo
Coordinator of this site? Confirm its status
PaviaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.