Registro Italiano Sclerosi Multipla e Patologie Correlate (Italian Multiple Sclerosis and Related Disorders Register)

26/11/2025
19/12/2025
Data source
Human
Disease registry
Access and validation

Governance details

Documents or webpages that describe the overall governance of the data source and processes and procedures for data capture and management, data quality check and validation results (governing data access or utilisation for research purposes).

Biospecimen access

Are biospecimens available in the data source (e.g., tissue samples)?

No

Access to subject details

Can individual patients/practitioners/practices included in the data source be contacted?

No

Description of data collection

In 2000, the Italian collection of MS clinical data started at different Italian MS centres in the framework of the Italian Multiple Sclerosis Database Network (MSDN). At the end of 2014, the Italian Multiple Sclerosis and Related Disorders Register (RISM) was set up to create a national data source collecting demographic and clinical data on people with multiple sclerosis.
Currently, data are collected through a web-based system - the RISM-App - developed ad hoc for the study. Each centre can enter the data after identification through a personalised password. In RISM, each patient is assigned to a specific centre and has a unique valid code identifier, obtained through the patient encrypted fiscal code.
The RISM-App includes 1,475 variables and is organised into sections and sub-sections. According to the current clinical practice, the following information is requested in the RISM-App: Identification/Personal data; Onset and Diagnosis (Anamnesis); Follow-up visits – EDSS, Safety; Relapses; Adverse events (clinical events); Treatments; Non-pharmacological treatments; Risk assessment; Pregnancies; COVID-19; Co-morbidity; Familiar anamnesis; Tests and scales; Laboratory exams; Magnetic Resonance, Liquor, Evoked Potentials; EEG, ECG, Blood pressure; Eye examination; Optical Computerised Tomography.
To harmonise data collection, the RISM-App integrates several standardised databases, including FarmaDati, MedDRA, ICD-9-CM, and EUROCAT (for congenital anomalies). Continuous data monitoring is ensured through regular communication with centres, biannual ad hoc reports providing both overall and centre-specific quality and descriptive indicators, data verification requests, and training on standardised data collection procedures. In addition, a set of built-in validation checks — such as consistency between date of birth, diagnosis, first visit, and treatment — is implemented in the RISM-App to prevent data inconsistencies.
Event triggering registration

Event triggering registration of a person in the data source

Disease diagnosis
Practice registration
Start of treatment

Event triggering de-registration of a person in the data source

Death
Emigration
Loss to follow up

Event triggering creation of a record in the data source

Clinical centers invite patients to be enrolled in RISM. After signing the informed consent of the study, a record is created to collect patients' demographic and clinical information.
Data source linkage

Linkage

Is the data source described created by the linkage of other data sources (prelinked data source) and/or can the data source be linked to other data source on an ad-hoc basis?

No
Data management specifications that apply for the data source

Informed consent for use of data for research

Possibility of data validation

Can validity of the data in the data source be verified (e.g., access to original medical charts)?

Yes

Data source preservation

Are records preserved in the data source indefinitely?

No

Data source preservation length

20 years

Approval for publication

Is an approval needed for publishing the results of a study using the data source?

Yes
Common Data Model (CDM) mapping

CDM mapping

Has the data source been converted (ETL-ed) to a common data model?

No