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Blood Pressure Target in Acute Stroke to Reduce hemorrhaGe After Endovascular Therapy

Not Applicable
Completed
Conditions
Cerebral Hemorrhage
Blood Pressure
Acute Stroke
Interventions
Other: Systolic blood pressure target < 130 mm Hg
Other: Systolic blood pressure target < 185 mm Hg
Registration Number
NCT03160677
Lead Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
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

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
320
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)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intensive blood pressure managementSystolic blood pressure target < 130 mm Hg-
Standard blood pressure managementSystolic blood pressure target < 185 mm Hg-
Primary Outcome Measures
NameTimeMethod
Rate of patients with intracranial hemorrhagic complicationsScan 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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (7)

Hôpital neurologique Pierre Wertheimer, Hospices Civils de Lyon

🇫🇷

Lyon, France

Hopital Foch

🇫🇷

Suresnes, France

CHU de Bordeaux

🇫🇷

Bordeaux, France

Centre Hospitalier Régional Universitaire

🇫🇷

Nancy, France

Hopital Lariboisière

🇫🇷

Paris, France

Fondation Ophtalmologique A de Rothschild

🇫🇷

Paris, France

Hopital de purpan

🇫🇷

Toulouse, France

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