- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00318578
Prognosis Factors Associated With Convulsive Status Epilepticus in Adults
Prognosis Factors Associated With Convulsive Status Epilepticus in Adults: A Multicenter Cohort Study
Study Overview
Status
Conditions
Detailed Description
Status epilepticus is a neurologic and medical emergency associated with high mortality and morbidity rates. According to the operational definition Convulsive Status Epilepticus (CSE) is defined as a single clinical seizure lasting more than 10 min, or two or more repeated seizures over a period of more than 10 minutes without intervening recovery of consciousness.
There are a few to date in literature reporting prognosis factors associated with this condition and, at this time, there are no published data considering an operational definition of CSE.
In a retrospective study considering an operational definition we identified a seizure duration of 15 min associated with poor outcome (not yet published).
The principal goal of this study is to evaluate factors associated with outcome in CSE, in particular seizure duration of more than 15 minutes.
The secondary goals are to evaluate the epidemiology and management at every stage of CSE thus redefined.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Abbeville, France, 80100
- Centre Hospitalier d'Abbeville
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Annonay, France, 07103
- Centre Hospitalier d'Annonay
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Argenteuil, France, 95100
- Centre Hospitalier Victor Dupouy
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Aulnay Sous Bois, France, 93
- Centre Hospitalier Robert Ballanger
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Cergy Pontoise, France, 95303
- Centre Hospitalier René Dubos
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Chartres, France, 28
- Centre Hospitalier de Chartres
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Châlons-en-Champagne, France, 51000
- Centre Hospitalier de Chalons-en-Champagne
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Clamart, France, 92140
- Centre Hospitalier Universitaire Antoine Beclere
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Clermont Ferrand, France, 63000
- Hôpital Gabriel Montpied
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Compiegne, France, 60200
- Centre Hospitalier de Compiegne
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Creteil, France, 94000
- Centre Hospitalier Universitaire Henri Mondor
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Dourdan, France, 91410
- Centre Hospitalier de Dourdan
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Dreux, France, 28102
- Centre Hospitalier de Dreux
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Grenoble, France, 38
- Centre hospitalier universitaire de Grenoble
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Le Chesnay, France, 78150
- Centre Hospitalier de Versailles
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Marseille, France, 13385
- Centre Hospitalier Universitaire La Timone
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Maubeuge, France, 59607
- Centre Hospitalier Sambre Avesnois
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Meaux, France, 77107
- Centre Hospitalier de Meaux
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Nancy, France, 54035
- Centre Hospitalier Universitaire de Nancy
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Nevers, France, 58000
- Centre Hospitalier Pierre Bérégovoy
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Nice, France, 06202
- Centre Hôspitalier ARCHET
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Niort, France, 79021
- Centre Hospitalier Georges Renon
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Orleans, France, 45067
- Centre Hospitalier Universitaire d'Orléans
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PAU, France, 64046
- Centre Hospitalier Francois Mitterrand
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Paris, France, 75000
- Centre Hospitalier Universitaire Cochin
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Paris, France, 75000
- Centre Hospitalier Universitaire Lariboisiere
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Paris, France, 75
- Centre Hospitalier Bichat Claude Bernard
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Paris, France, 75
- Fondation Hôpital Saint Joseph
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Pessac, France, 33600
- Clinique Mutualiste de Pessas
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Poitiers, France
- Centre Hospitalier Universitaire de Poitiers
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Roanne, France, 42328
- Centre Hospitalier de Roanne
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Rodez, France, 12
- Centre Hospitalier de Rodez
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Saint Lo, France, 50000
- Centre Hospitalier Mémorail France Etats Unis Saint Lo
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Suresnes, France, 92151
- Centre Hospitalier Foch
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- More than 18 years old
- Convulsive status epilepticus according to operational definition as any seizure lasting for 10 minutes or longer, or two or more intermittent seizures lasting for greater than 10 minutes from which the patient did not regain consciousness.
- Beginning of seizure less than 12 hours before intensive care unit admission
- Convulsive status epilepticus occurring during intensive care unit stay
Exclusion Criteria:
- Less than 18 years old
- Patients that seized up to 9 minutes
- Beginning of seizure more than 12 hours before intensive care unit admission
Study Plan
How is the study designed?
Design Details
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Stephane LEGRIEL, MD, Versailles Hospital
- Principal Investigator: Bruno MOURVILLIER, MD, Centre Hospitalier Bichat Claude Bernard
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- LEGRIEL stephane
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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