Actively Recruiting
Study of Pathophysiology of Status Epilepticus and Dysimmune Encephalitis
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-02-04
400
Participants Needed
1
Research Sites
339 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
COLETTE is an interventional study for which blood, cerebrospinal fluid and post-mortem tissues are collected in patients with status epilepticus or epilepsy associated to dysimmune encephalitis as well as in control patients, to better understand the pathophysiology of these severe epileptic disorders.
CONDITIONS
Official Title
Study of Pathophysiology of Status Epilepticus and Dysimmune Encephalitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 2 years or older with status epilepticus (Group 1)
- Patients aged 2 years or older with epilepsy linked to dysimmune encephalitis (Group 2)
- Patients aged 18 years or older without status epilepticus or dysimmune encephalitis (Group 3)
- Affiliation to a French social security system excluding "Aide Médicale" Etat (AME)
- Patients or their relatives have given free, informed, written consent
- Patients may be under legal protection (guardianship, curatorship) or not
You will not qualify if you...
- Women who are pregnant or clinically detected as pregnant (Groups 1, 2, and 3)
- Patients deprived of liberty (all groups)
- Patients with known neurodegenerative disease (Groups 1 and 3)
- Patients already treated by corticosteroids or intravenous immunoglobulins (Group 2)
- Patients with status epilepticus (Group 3)
- Patients with brain tumor, severe head trauma, meningitis, subarachnoid hemorrhages, or stroke (Group 3)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hôpital de la Pitié Salpêtrière
Paris, France, 75013
Actively Recruiting
Research Team
V
Vincent NAVARRO, Pr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
3
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