Social and Prognostic Inequalities in Patients Hospitalised for Cerebrovascular Accident (CVA) in Four Contrasting French Departments

NCT ID: NCT01906463

Last Updated: 2018-12-27

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 1612 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2011-07-31
• Study Completion Date: 2015-10-31

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 population of persons aged over 60 years and the foreseeable changes in lifestyle will increase the burden of this disease, in particular since the region is marked by a high prevalence of arterial hypertension and diabetes and a high level of precarity. In addition, this study will provide epidemiological information on CVA, its risk factors and management, which are non-existent for the department of French Guyana where the health environment is manifestly insufficient. These data should make it possible to better evaluate the resources available and the healthcare needs in Guyana.

Conditions

Symptomatic CVA (de Novo CVA)

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• 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 Criteria

• - 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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier Universitaire Dijon

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CHU de Dijon

Dijon, , France

Countries

France

Other Identifiers

bonithon PHRC N 2010

Identifier Type: -

Identifier Source: org_study_id