Efficacy and Safety of Antihypertensive Treatment With Mobile Stroke Units in Ultra-Early Intracerebral Hemorrhage

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorXuanwu Hospital, Beijing

About this trial

MSU-ICH is a prospective, multicenter, Week-wise-randomized, open-label, blinded-endpoint (PROBE) clinical trial comparing ultra-early prehospital blood pressure lowering delivered by a Mobile Stroke Unit (MSU) with standard Emergency Medical Services (EMS) in patients with spontaneous intracerebral hemorrhage.

Eligibility criteria

Qualifiers

History and physical/neurological examination consistent with acute stroke.

Age ≥18 years;

Time from symptom onset to enrollment <3 hours (onset defined as last known normal).

Systolic blood pressure ≥150 mmHg and ≤220 mmHg;

Disqualifiers

Glasgow Coma Scale (GCS) score ≤5.

Contraindications to intensive blood pressure lowering, including severe arterial stenosis or high-grade stenotic valvular heart disease.

Malignant disease or other serious primary illness with a life expectancy of <3 months.

Current participation in another interventional randomized clinical trial.

Trial design

Treatments tested in this trial

  • Mobile Stroke Unit Management
  • Standard Management

Treatment groups

706 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Xuanwu Hospital, Beijing

Lead sponsor

Beijing Emergency Medical Center

Collaborator

Huizhou Third People's Hospital, Guangzhou Medical University

Collaborator

Suzhou First People's Hospital

Collaborator

Nanyang nanshi Hospital

Collaborator