Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
300

Summary

Conditions
  • Acute Stroke
  • Blood Pressure
  • Cerebral Hemorrhage
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Patients will be followed for 72 hours: inclusion after reperfusion: clinical evaluation with NIHSS (National Institute of Health Stroke Score) score, measurement of blood pressure. within 24 hours after reperfusion: blood pressure measurements at 24 hours: NIHSS score. Between 24 and 36 hours :cere...

Patients will be followed for 72 hours: inclusion after reperfusion: clinical evaluation with NIHSS (National Institute of Health Stroke Score) score, measurement of blood pressure. within 24 hours after reperfusion: blood pressure measurements at 24 hours: NIHSS score. Between 24 and 36 hours :cerebral scan (assessment of hemorrhagic transformations and cerebral infarction volumes). 72 hours after reperfusion: brain scanner in case of hyperdensity on the initial scanner

Tracking Information

NCT #
NCT03359434
Collaborators
Not Provided
Investigators
Principal Investigator: MAZIGHI Mikael, MD PhD Fondation Ophtalmologique A. de Rothschild