Study of the Rate of Progression of Cerebral Ischemia in Afro-Caribbeans
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de la Guadeloupe
About this trial
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.
Eligibility criteria
Qualifiers
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.
Emergency inclusion, with exemption from obtaining consent due to the immediate life-threatening emergency situation of the patient (Article L1122-1-3 of the French Public Health Code); as soon as possible, consent to continue will be sought from the patient or, if applicable, from a relative or a trusted person.
Disqualifiers
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
Trial design
Treatments tested in this trial
- No Interventions
Treatment groups
135 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov