Status:
COMPLETED
Social and Prognostic Inequalities in Patients Hospitalised for Cerebrovascular Accident (CVA) in Four Contrasting French Departments
Lead Sponsor:
Centre Hospitalier Universitaire Dijon
Conditions:
Symptomatic CVA (de Novo CVA)
Eligibility:
All Genders
18+ years
Brief Summary
This study should also raise questions about the interest and feasibility of establishing a permanent registry of CVA in the Antilles and Guyana. Indeed in coming decades, the expected doubling of the...
Eligibility Criteria
Inclusion
- Pre- inclusion
- Patients who have received information about the study (directly or via a person of trust),
- Patients aged more than 18 years,
- Patient hospitalised for a suspected first symptomatic CVA (whatever the mechanism), preceded or not by a transient ischemic attack (TIA),
- Patients with a cerebral imaging examination (CT-scan and/or MRI),
- in Guyana, suspicion of a first CVA according to WHO clinical criteria and who died before the authorised images for descriptive purposes,
- Patients able to answer questions personally or through a parent or a person of trust.
- Definitive inclusion
- \- Patients with confirmed CVA diagnosed according to clinical criteria (WHO criteria) and imaging criteria.
Exclusion
- \- Patients who refuse to take part in the study,
- Patients with prior symptomatic CVA,
- Patients without cerebral imaging (except in Guyana, for patients with suspected CVA who died before imaging),
- Patients with another severe evolutive disease that could cause death in the weeks following the CVA,
- Patients who cannot be contacted by telephone at 1 month.
Key Trial Info
Start Date :
July 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2015
Estimated Enrollment :
1612 Patients enrolled
Trial Details
Trial ID
NCT01906463
Start Date
July 1 2011
End Date
October 1 2015
Last Update
December 27 2018
Active Locations (1)
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1
CHU de Dijon
Dijon, France, 21079