CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 404 enrolled
Drug / intervention
Labetalol Hydrochloride +10 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00226096
NCT00226096N/ACompleted

A Randomised Trial to Establish the Effects of Early Intensive Blood Pressure Lowering on Death and Disability in Patients With Stroke Due to Acute Intracerebral Haemorrhage

The George Institute·interventional·Posted Sep 26, 2005·Updated Jun 26, 2008

In Brief

A clinical study evaluating Labetalol Hydrochloride, Metoprolol tartrate, and 9 other interventions for CVA (Cerebrovascular Accident) and 2 related conditions. Completed, enrolled 404 participants across 20 sites in 3 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, China, New Zealand

Timeline

N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 26, 2005
Enrollment StartNov 1, 2005
Primary CompletionSep 1, 2007
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 20.8 years ago

Interventions

Labetalol Hydrochloridedrug

Metoprolol tartratedrug

Hydralazine Hydrochloridedrug

Glycerol Trinitratedrug

Phentolamine mesylatedrug

Nicardipinedrug

Urapidildrug

Esmololdrug

Clonidinedrug

Enalaprilatdrug

Nitroprussidedrug