I63 I60 I61
Conditions
Interventions
Group 1: Children and adolescents (>28 days of life, < 18 years) with ischemic or hemorrhagic stroke.
Data are collected at the initial stroke event (including clinical presentation, risk factors/etio
there will be no additional appointments.
Questionnaire-based data are collected on quality of life (after 6 months, 12 months, then annually) and behaviour (after 12 months).
Sponsors
LMU Klinikum
Eligibility
Sex/Gender
All
Age
29 Days to 18 Years
Inclusion criteria
Inclusion criteria: ischemic or hemorrhagic stroke (index stroke or recurrent stroke)
Exclusion criteria
Exclusion criteria: 1. neonatal/perinatal stroke 2. suspected perinatal stroke with diagnosis beyond the neonatal period 3. traumatic intracranial hemorrhage 4. secondary infarction (hemorrhagic or ischemic) of a sinus vein thrombosis 5. No informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Registry - systematic data collection The primary objective of PRiSMA is the systematic, prospective and longitudinal collection of data on pediatric stroke patients | — |
Secondary
| Measure | Time frame |
|---|---|
| registry | — |
Countries
Austria, Germany
Contacts
Public ContactLucia Gerstl
LMU Klinikum
Outcome results
None listed