NCT07230925

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
135

participants targeted

Target at P50-P75 for all trials

Timeline
20mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress17%
Jan 2026Jan 2028

First Submitted

Initial submission to the registry

November 14, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

November 17, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2028

Last Updated

November 17, 2025

Status Verified

October 1, 2025

Enrollment Period

2 years

First QC Date

November 14, 2025

Last Update Submit

November 14, 2025

Conditions

Keywords

Cerebrovascular accidentCerebral Blood Flow

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

Other: No Interventions

Patients residing in Nantes

Patients residing in Nantes

Other: No Interventions

Interventions

No interventions

Patients residing in GuadeloupePatients residing in Nantes

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

Biospecimen

Retention: SAMPLES WITH DNA

blood sample

MeSH Terms

Conditions

Ischemic StrokeBrain IschemiaStroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Donald ACCROMBESSI, Doctor

    CHU de la Guadeloupe

    PRINCIPAL INVESTIGATOR
  • Valérie BASSIEN CASPA, PHD

    CHU de la Guadeloupe

    STUDY CHAIR

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

Locations