Study of the Rate of Progression of Cerebral Ischemia in Afro-Caribbeans
VESPERALS
1 other identifier
observational
135
1 country
1
Brief Summary
To compare the progression of cerebral ischemia from HF in Afro-Caribbean patients admitted to the CHUG to that of patients from Nantes included in the national ETIS registry.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 14, 2025
CompletedFirst Posted
Study publicly available on registry
November 17, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2028
November 17, 2025
October 1, 2025
2 years
November 14, 2025
November 14, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
progression of cerebral ischemia of IC in Afro-Caribbean patients admitted to the CHUG with that of patients from Nantes included in the national register ETIS
Compare the progression of cerebral ischemia of IC in Afro-Caribbean patients admitted to the CHUG with that of patients from Nantes included in the national register ETIS
baseline, day 1,2,3,4 an day 90
Secondary Outcomes (3)
Characterizing the profile of Afro-Caribbean patients
baseline
Characterizing the profile of Afro-Caribbean patients
baseline
Characterizing the profile of Afro-Caribbean
at the end of the suty
Study Arms (2)
Patients residing in Guadeloupe
Patients residing in Guadeloupe
Patients residing in Nantes
Patients residing in Nantes
Interventions
Eligibility Criteria
patients with a diagnosis of stroke from LVO identified by medical imaging
You may qualify if:
- Patients aged 18 and over, admitted for IC due to LVO verified by medical imaging and hospitalized in neurology.
- Patients residing in Guadeloupe
- Afro-Caribbean patients: of African ancestry.
- Patients affiliated to a social security scheme or equivalent
You may not qualify if:
- Patients under 18 years old
- Non-resident patients in Guadeloupe
- Protected persons (articles L1121-5, L1121-6 and L121-8 of the Public Health Code): pregnant or breastfeeding women, persons deprived of their liberty, under guardianship or curatorship)
- Withdrawal of consent during the study
- Patients not affiliated to a social security or equivalent scheme
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre Hospitalier Universitaire de la Guadeloupe
Pointe-à-Pitre, Guadeloupe, 97159, Guadeloupe
Biospecimen
blood sample
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Donald ACCROMBESSI, Doctor
CHU de la Guadeloupe
- STUDY CHAIR
Valérie BASSIEN CASPA, PHD
CHU de la Guadeloupe
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 14, 2025
First Posted
November 17, 2025
Study Start
January 1, 2026
Primary Completion (Estimated)
January 1, 2028
Study Completion (Estimated)
January 1, 2028
Last Updated
November 17, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share