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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05598138
Other study ID # 2020/CHU/40
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 22, 2021
Est. completion date June 21, 2023

Study information

Verified date July 2023
Source Centre Hospitalier Universitaire de la Réunion
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cross-sectional regional multicenter hospital study of all neurological events (stroke, AIT and mimics) for diagnostic and prognostic purposes. Cost of illness study.


Recruitment information / eligibility

Status Completed
Enrollment 795
Est. completion date June 21, 2023
Est. primary completion date June 21, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - affiliated to a social security scheme - clinical signs suggestive of stroke : hemiparesis or hemiplegia, unilateral sensory disorder, language disorder, balance disorder, dizziness, loss of total or partial bilateral or monocular vision, sudden neurological deficit Exclusion Criteria: - current pregnancy - Recent clinical history of head trauma - patients aged < 18 years old - patient under guardianship or curatorship - Person deprived of liberty

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Biological Collection
A blood sample (10 ml) will be taken for each patient included in the study.

Locations

Country Name City State
Réunion CHU de La Réunion Saint-Denis
Réunion CHU de La Réunion Saint-Pierre

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de la Réunion

Country where clinical trial is conducted

Réunion, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinico-biological score area under the diagnostic score curve identifying ischemic stroke, stroke hemorrhagic or mimics. 24 hours after the stroke
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