Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage

NCT00226096 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 404

Last updated 2008-06-26

No results posted yet for this study

Summary

The purpose of the study is to determine whether lowering high blood pressure levels after the start of a stroke caused by bleeding in the brain (intracerebral haemorrhage) will reduce the chances of a person dying or surviving with a long term disability. The study will be undertaken in two phases: a vanguard phase in 400 patients, to plan for a main phase in 2000 patients.

Conditions

  • CVA (Cerebrovascular Accident)
  • Cerebral Hemorrhage
  • Intracranial Hemorrhages

Interventions

DRUG

Labetalol Hydrochloride

DRUG

Metoprolol tartrate

DRUG

Hydralazine Hydrochloride

DRUG

Glycerol Trinitrate

DRUG

Phentolamine mesylate

DRUG

Nicardipine

DRUG

Urapidil

DRUG

Esmolol

DRUG

Clonidine

DRUG

Enalaprilat

DRUG

Nitroprusside

Sponsors & Collaborators

  • National Health and Medical Research Council, Australia

    collaborator OTHER
  • The George Institute

    lead OTHER

Principal Investigators

  • Craig Anderson, PhD · The George Institute

  • Bruce Neal, PhD · The George Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-11-30
Primary Completion
2007-09-30
Completion
2007-09-30

Countries

  • Australia
  • China
  • New Zealand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00226096 on ClinicalTrials.gov