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ARTEMIS - The ARTEMIS Cohort
Sponsor: Vastra Gotaland Region
Summary
This multinational European observational clinical study focuses on non-progressive congenital ataxia (NPCA), a very rare early-onset neurological condition also within the cerebral palsy (CP) concept as ataxic CP. The study aims to improve the diagnosis and care of affected children through a comprehensive approach that integrates detailed clinical assessments, brain imaging analyses, and advanced genetic testing. By identifying developmental trajectories, specific impairment profiles, brain MRI patterns, and genetic variants, the researchers aim to elucidate underlying mechanisms, origins and clinical heterogeneity of NPCA. The study also assesses the broader impact of the condition on the quality of life of affected children and the associated burden on their families. Preliminary data found a high prevalence of cognitive and neuropsychiatric impairments, and a frequent lack of identifiable brain lesions on MRI, raising the hypothesis of a strong genetic contribution.
Official title: Non-progressive Congenital Ataxia - Advancing Diagnosis to Enhance Chances for Targeted Therapy
Key Details
Gender
All
Age Range
5 Years - 8 Years
Study Type
OBSERVATIONAL
Enrollment
50
Start Date
2026-04
Completion Date
2027-12-31
Last Updated
2026-02-19
Healthy Volunteers
No
Locations (7)
KU Leuven
Leuven, Belgium
Aarhus University Hospital
Aarhus, Denmark
Toulouse University Hospital
Toulouse, France
University Hospital Tübingen
Tübingen, Germany
IASO Children's Hospital
Athens, Greece
Vestfold Hospital Trust
Tønsberg, Norway
Queen Silvia Children's Hospital at Sahlgrenska University Hospital
Gothenburg, Sweden