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Brief Title: A Registry of AL Amyloidosis (ReAL)
Official Title: A Registry to Investigate Real-world Natural History, Impact of Therapies and Patterns of Progression of AL Amyloidosis (ReAL)
Study ID: NCT04839003
Brief Summary: The purpose of this protocol is to generate a large registry of patients with AL amyloidosis.
Detailed Description: Thanks to this registry, it will be possible to collect data at diagnosis and during follow up, in order to be able to describe the natural history of AL amyloidosis in a real-world setting and to define and validate prognostic models, response and relapse criteria applicable at any point of the disease.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Fondazione IRCCS Policlinico San Matteo, Pavia, , Italy