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Clinical Trials/NCT00763217
NCT00763217
Completed
Not Applicable

Characterization of Clinical, Biological and Pharmacological Markers of Stroke Outcome

University Hospital, Lille1 site in 1 country550 target enrollmentJune 2005
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
University Hospital, Lille
Enrollment
550
Locations
1
Primary Endpoint
severity of stroke measured by NIH severity score
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

In a previous suty, we have demonstrated that prior transient ischemic attack, treatment lipid-lowering drug or physical activity are associated to a better outcome of stroke. The aim of the study is to understand the mechanisms of this preventive neuroprotection by establishing link between biomarkers and preventive and neuroprotective measures.To answer to the question, we conduct a cohort study of stroke patients.

Detailed Description

In the cohort, the severity of stroke (NIHSS) will be correlated with : * clinical factors, * pharmacological factors, * biological factors (inflammatory markers, hemostasis...)

Registry
clinicaltrials.gov
Start Date
June 2005
End Date
June 2012
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Lille
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ischemic or hemorrhage stroke
  • hemispheric stroke
  • stroke dating from less 48h

Exclusion Criteria

  • non hemispheric stroke
  • malformative intracranial hemorrhage
  • traumatic intracranial hemorrhage
  • subarachnoidal hemorrhage

Outcomes

Primary Outcomes

severity of stroke measured by NIH severity score

Time Frame: inclusion, day7, month3, year3

Secondary Outcomes

  • clinical, pharmacological and biological (metabolic, inflammation, hemostasis...) cognitive status(inclusion and year3)

Study Sites (1)

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