Clinical Biological and Pharmacological Factors Influencing Stroke Outcome (BIOSTROKE)

Principal Investigator

Régis Bordet
Department of Pharmacology,
University of Lille,
INSERM
U1171, 59045 Lille, France.
regis.bordet@univ-lille2.fr

Summary

Country France
Principal Investigator Régis Bordet
Contact person (email) regis.bordet@univ-lille2.fr
Key publication/reference Ducroquet et al. Stroke 2013;44:2324-2326
Clinicaltrial.gov: NCT00763217
Years in which study conducted 2005-2015
Sample  
Size 477 included patients/210 patients reviewed or assessed by phone at 5 years
Population: Hospital/community Hospital
Selection: consecutive/random Consecutive
Admit with previous stroke? Yes
Admit with TIA? Yes
Age range 53-80
Number of centres 1
Control group: number, population, selection No
Assessment  
Initial: Time and data collected/tests administered Within 7 days: MedHx, VRF, MRI, plasma analysis, MMSE, IQCODE, CT
Detailed (initial)
Subsequent (follow-ups) 3m: function, IQCODE, MMSE
5 years: extensive NΨ; biological samples
Stroke-related data NIHSS , TOAST 
Functional tests/data Modified Rankin Scale, Barthel Index
Other medical tests/data Plasma biomarkers (vascular, inflammation, trophic factors, AD markers); DNA
Neuropsychological tests Test battery, MoCA
MRI scans, when and how many Initial, 5 year
PET scans No
Psychiatric exams/diagnoses Depression  (CES-D), apathy (Lille Apathy Rating Scale), anxiety (Hamilton Anxiety Scale), fatigue
Intervention trialled? No

CT=computed tomography scan, MedHx=medical history, VRF=vascular risk factors (hypertension, diabetes, atrial fibrillation, obesity, smoking etc.), NΨ=neuropsychological, TIA=transient ischemic attack, m=month, y=year