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Clinical Trial Summary

Epidemiological data collection of adult patients affected by myelodysplastic syndrome (MDS) newly diagnosed.


Clinical Trial Description

Development of an Italian regional registries MDS network using the same electronic case report form for data storage, with the following broad aims: - Ability to aggregate and process anonymous epidemiological data collected by individual regional registers; - Ability to aggregate the available data with those of other international registries existing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02808858
Study type Observational [Patient Registry]
Source Fondazione Italiana Sindromi Mielodisplastiche-ETS
Contact Valeria Santini, Prof.
Phone 013120
Email segreteriafismonlus@ospedale.al.it
Status Recruiting
Phase
Start date September 2013
Completion date May 2032

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