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Predicting Outcome and Disease Course in acquired demyelinating syndromes in childhood

Predicting Outcome and Disease Course in acquired demyelinating syndromes in childhood - PROUD-kids 2.0

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55633
Enrollment
1200
Registered
2017-10-20
Start date
2017-10-01
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
No minimum to 17 Years

Inclusion criteria

Inclusion criteria: Patients 1. Age under 18 years 2. Auto-immune mediated, demyelinating disorder of the CNS 3. No other suspected disease causing demyelination in the CNS 4. Written informed consent is obtained of parents or caregivers. In case the patient is 12 years of age or older, the patient needs to provide written informed consent as well. , Healthy controls 1. Age under 18 years 2. No known systemic auto-immune disease 3. Full siblings (same father and same mother) of the patient are eligible and not blood-related children sharing similar environments (school, neighbourhood etc). 4. Written informed consent is obtained , Other neurological diseases (OND): Patients will be included at the outpatient clinics of pediatric neurologists at Erasmus MC-Sophia. 1. Age under 18 years 2. No systemic auto-immune disease that might cause inflammatory disease in the CNS 3. Written informed consent is obtained of parents or caregivers. In case the child is 12 years of age or older, the child needs to provide written informed consent as well.

Exclusion criteria

Exclusion criteria: 1) Age of onset above 18 years 2) Inflammation in the CNS by other causes than ADS (for example systemic lupus erythematosus, Sj*gren syndrome, sarcoidosis,). 3) If written informed consent is not obtained. 4) Withdrawal from study by patient and/or parents.

Design outcomes

Primary

MeasureTime frame
- Identifying prognostic factors for disease course and severity - Identification of specific ADS subgroups - Role of environmental and genetic factors in MS and other ADS - Estimating incidence and prevalence of ADS subtypes in the Netherlands. - Accurate and suitable parameters expressing disease severity for pediatric ADS

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)