Acute Stroke, Blood Pressure, Cerebral Hemorrhage
Conditions
Keywords
Acute Stroke, Blood Pressure, Cerebral Hemorrhage
Brief summary
A randomized, multicenter study comparing two strategies: 1 / standard management of systolic blood pressure according to international recommendations (systolic blood pressure \<185 mm Hg) versus 2 / intensive blood pressure management Systolic with a target \<130 mm Hg.
Detailed description
Patients will be followed for 3 months: * 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: measurement of blood pressure (T0 + 24 h and evaluation of the NIHSS score. * Between 24 and 36 hours :cerebral scan (assessment of hemorrhagic transformations and cerebral infarction volumes). For some centers: Cerebral MRI without injection between H24 and H36 * 72 hours after reperfusion: Cerebral scanner in case of hyperdensity on the initial scanner * 3 months after reperfusion: disability assessment by Rankin score
Interventions
Adaptation of antihypertensive treatments to reach the Systolic blood pressure target \< 130 mm Hg
Adaptation of antihypertensive treatments to reach the Systolic blood pressure target \< 185 mm Hg
Sponsors
Study design
Eligibility
Inclusion criteria
* Intracranial Occlusion of internal carotid arteries and/or proximal middle cerebral (segment M1) diagnosis made on initial Imaging. * Reperfusion after a thrombectomy procedure (defined by a 2b-3 TICI score -Thrombolysis In Cerebral Infarction- score).
Exclusion criteria
* Per-procedure hemorrhagic complications (prior to reperfusion) * Systolic blood pressure at baseline \<130 mm Hg within one hour of recanalization * Pre-existing stroke handicap defined by a Rankin score (modified scale, mRS)\> 3 * Hemodynamically significant carotid stenosis * Occlusion of the isolated cervical carotid artery * Known pregnancy * Legal protection * Non-affiliation to a social security scheme * Refusal of the patient (or of his / her relatives in case of urgent inclusion)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of patients with intracranial hemorrhagic complications | Scan performed between 24 and 36 hours after thrombectomy | Rate of patients with intracranial hemorrhagic complications (Symptomatic or asymptomatic) on cerebral scan, evaluated with a double centralized blind reading |
Countries
France