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Clinical Trials/ACTRN12607000591459
ACTRN12607000591459
Completed
Phase 4

A randomised clinical trial to compare the efficacy of intravenous droperidol and olanzepine as adjuncts to midazolam for sedation of the severely agitated patient

Austin Hospital0 sites320 target enrollmentNovember 16, 2007
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Conditionssevere agitationMental Health - Other mental health disordersOther - Conditions of unknown or disputed aetiology (such as chronic fatigue syndrome/myalgic encephalomyelitis)

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
severe agitation
Sponsor
Austin Hospital
Enrollment
320
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 16, 2007
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Austin Hospital

Eligibility Criteria

Inclusion Criteria

  • •Emergecncy department patients who require chemical sedation as determined by an Emergency Physician or a senior registrar.

Exclusion Criteria

  • •known hypersensitivity to midazolam, droperidol or olanzepine, reversible aetiology for agitation (hypotension, hypoxia, hypoglycaemia), known pregnancy, acute alcohol withdrawal.

Outcomes

Primary Outcomes

Not specified

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