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Clinical Trials in France / NCT07172542
Starting soon Observational

High Risk of Death or Disability in Brain Hemorrhage: Role of Spot Sign and Secondary Markers

NCT07172542 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier de Gonesse
Phase
Observational
Started
2025-10-15
Last updated
2025-09-15

Condition(s) studied

Intracerebral HemorrhageCerebral HemorrhageStrokeBrain Injuries

Study summary

This study looks at patients with brain hemorrhage to see if a special sign on brain scans, called the "Spot Sign," combined with other scan features, can predict a higher risk of death or disability. By comparing patient outcomes with existing prediction scores, the study aims to understand whether these scan markers provide extra value in identifying patients at higher risk.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Spontaneous intracerebral hemorrhage confirmed by contrast-enhanced CT scan. * Follow-up CT scan performed within 24 to 48 hours. Non-inclusion Criteria : * Absence of initial contrast-enhanced CT or follow-up CT. * Hematoma due to trauma, epidural hematoma (EDH), subdural hematoma (SDH), or subarachnoid hemorrhage (SAH). Exclusion Criteria: * Patient deceased before the initial contrast-enhanced CT. * Major missing clinical data.

Primary outcome measure(s)

  • Hematoma Expansion within 48 Hours: Increase of more than 6 mL or over 30% between the initial CT and the follow-up CT (PREDICT study criterion) and/or Occurrence of Death Within the First Month — 48 hours

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier de Gonesse Gonesse France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07172542 on ClinicalTrials.gov ↗ ← All trials in France