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Clinical Trials/JPRN-UMIN000006526
JPRN-UMIN000006526
Completed
未知

Antihypertensive Treatment in Acute Cerebral Hemorrhage-II - ATACH-II

niversity of Minnesota National Cerebral and Cardiovascular Center0 sites1,000 target enrollmentOctober 14, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
Cerebral Hemorrhage
Sponsor
niversity of Minnesota National Cerebral and Cardiovascular Center
Enrollment
1000
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

We conducted a multicenter trial where eligible subjects with ICH were randomized to intensive (<140 mm Hg) and standard (<180 mm Hg) SBP reduction in a 1:1 ratio <4.5h. The primary outcome of death and disability was ascertained at 3-M post randomization. Compared with standard SBP reduction, intensive SBP reduction in patients with ICH did not lower the rate of death and disability despite achieving a small magnitude reduction in hematoma expansion.

Registry
who.int
Start Date
October 14, 2011
End Date
September 14, 2015
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Minnesota National Cerebral and Cardiovascular Center

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\.ICH is due to previously known neoplasms, AVM, or aneurysms 2\.Intracerebral hematoma considered to be related to trauma 3\.ICH located in infratentorial regions such as pons or cerebellum 4\.IVH associated with intraparenchymal hemorrhage and blood completely fills one lateral ventricle or more than half of both ventricles 5\.Patient to receive immediate surgical evacuation 6\.Current pregnancy, parturition within previous 30 days or active lactation 7\.Use of warfarin within the last 5 days and INR \>4 8\.A platelet count less than 50,000/mm3 9\.Known sensitivity to nicardipine 10\.Pre\-morbid disability requiring assistance in ambulation or activities of daily living 11\.Subjects living will precludes aggressive ICU management 12\.Subject is currently participating in another interventional clinical trial

Outcomes

Primary Outcomes

Not specified

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