ACTRN12614000980639
Completed
Phase 4
A randomised clinical trial to compare the efficacy of the intravenous midazolam-droperidol combination, droperidol only and olanzepine only for sedation of the severely agitated patient
Austin Hospital0 sites342 target enrollmentSeptember 12, 2014
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Austin Hospital
- Enrollment
- 342
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Emergency Department patients aged 18\-65 years who require IV drug sedation for acute agitation
Exclusion Criteria
- •1\. known hypersensitivity or contraindication to the study drugs
- •2\. reversible aetiology for agitation (hypotension, hypoxia, hypoglycaemia)
- •3\. known pregnancy
- •4\. acute alcohol withdrawal (particularly amenable to benzodiazepines alone)
Outcomes
Primary Outcomes
Not specified
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