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INTEnsive care bundle with blood pressure Reduction in Acute Cerebral haemorrhage Trial

An investigator initiated and conducted, international, multicentre, stepped wedge cluster randomised study of a care bundle of physiological control strategies in acute intracerebral haemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOC-17011787
Enrollment
Unknown
Registered
2017-06-28
Start date
2017-10-16
Completion date
Unknown
Last updated
2017-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intracerebral Hemorrhage

Interventions

intensive care bundle group:goal-directed care bundle of active management
Usual care group:NA

Sponsors

The George Institute For Global Health At Peking University Health Science Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. aged =18 years; 2. Acute stroke syndrome that is due to presumed spontaneous ICH, confirmed by clinical history and a CT scan without/without contrast, and if an CT angiogram is also undertaken as part of routine care; 3. Presentation to hospital within 6 hours of stroke onset.

Exclusion criteria

Exclusion criteria: 1. Definite evidence that the ICH is secondary to a structural abnormality in the brain or previous thrombolysis; 2. A high likelihood that the patient will not adhere to the study treatment and follow-up regimen; 3. In each case, the decision about the patients eligibility will be based on the attending clinicians interpretation of the above eligibility criteria.

Design outcomes

Primary

MeasureTime frame
a shift analysis of mRS scores;

Secondary

MeasureTime frame
a shift analysis of NIHSS scores;Death and disability (mRS 3-6);Death;Disability(mRS 3-5);EQ-5D;Duration of hospitalisation;

Countries

China

Contacts

Public ContactCraig Anderson

The George Institute For Global Health At Peking University Health Science Center

canderson@georgeinstitute.org.cn+86 010 82800577 ext 557

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 7, 2026