A Registry to Investigate Real-world Natural History, Impact of Therapies and Patterns of Progression of AL Amyloidosis (ReAL)
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
The purpose of this protocol is to generate a large registry of patients with AL amyloidosis.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
Italy
Fondazione IRCCS Policlinico San Matteo
RECRUITING
Pavia
Time Frame
Start Date: 2020-02-27
Estimated Completion Date: 2025-05
Participants
Target number of participants: 5000
Related Therapeutic Areas
Sponsors
Leads: Fondazione IRCCS Policlinico San Matteo di Pavia