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Oral Olanzapine Versus Haloperidol or Diazepam

Primary Purpose

Acute Agitation, Behavioural Emergency

Status
Terminated
Phase
Phase 4
Locations
Hong Kong
Study Type
Interventional
Intervention
Olanzapine oro-dispersible 5Mg Tab
Haloperidol 2Mg encapsulated Tab
Diazepam 2Mg encapsulated Tab
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Agitation focused on measuring emergency, emergency medicine, sedation, acute agitation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Accident & Emergency Department patients
  • Requiring oral drug sedation (as determined by an emergency clinician) will be enrolled.

Exclusion Criteria:

  • known hypersensitivity or contraindication to the study drugs
  • reversible aetiology for agitation (e.g. hypotension, hypoxia, hypoglycaemia)
  • known pregnancy
  • acute alcohol withdrawal
  • refusal to take oral medication
  • patients from correctional facilities

Sites / Locations

  • Queen Elizabeth Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Olanzapine

Haloperidol

Diazepam

Arm Description

oro-dispersible tablet (wafer)(Zyprexa), 5 mg, single dose

Haloperidol encapsulated tablet, 2 mg tablet, single dose

Diazepam encapsulated tablet, 2mg tablet, single dose

Outcomes

Primary Outcome Measures

Time to achieve adequate sedation
Adequate sedation is determined by a 6-point validated scale

Secondary Outcome Measures

Total study drug doses administered; alternative drugs and doses used
Corrected QT interval (QTc)
AED length of stay (LOS)
Adverse events
including airway management (jaw thrust, oral, nasal airway), need for assisted ventilation (bag/mask, intubation), oxygen desaturation <90%, systolic BP<90 mmHg, dystonic reactions, seizures, vomiting or aspiration

Full Information

First Posted
August 8, 2017
Last Updated
November 3, 2022
Sponsor
The University of Hong Kong
Collaborators
Queen Elizabeth Hospital, Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT03246620
Brief Title
Oral Olanzapine Versus Haloperidol or Diazepam
Official Title
Oro-dispersible Olanzapine (Wafer) Versus Conventional Oral Haloperidol or Diazepam Tablets for the Management of Acute Agitation in the Accident and Emergency Department - a Multicentre Randomised Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Terminated
Why Stopped
The study was terminated prematurely due to difficulties in patient recruitment and associated potential for selection bias.
Study Start Date
September 1, 2017 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
June 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
Collaborators
Queen Elizabeth Hospital, Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether oral olanzapine is safer (fewer adverse events) and more effective (shorter time to sedation) than conventional haloperidol or diazepam when used in the management of acute agitation in the emergency.
Detailed Description
Investigate oral use of sedating drugs within a predominantly Chinese population, to address this void in international literature impacting the management of acute agitation. The multi-centre Randomised Clinical Trial will determine the safety and efficacy of oral olanzapine, in comparison with conventional medicines (haloperidol or diazepam) in a three-arm comparison for the sedation of acutely agitated patients in AEDs. Specifically, we aim to determine if administration of oral olanzapine (a)is more effective than sedation with oral haloperidol or oral diazepam alone; (b)is safer than sedation with comparison arms; (c)decreases the amount of subsequent redosing or alternative drugs required; (d)is more favourable than the haloperidol and diazepam arms with respect to safety, efficacy and adverse events. Investigate potential variables leading to AED attendance and/or admission requiring oral sedation. These may include patient demographic and regular medications and adherence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Agitation, Behavioural Emergency
Keywords
emergency, emergency medicine, sedation, acute agitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Olanzapine
Arm Type
Experimental
Arm Description
oro-dispersible tablet (wafer)(Zyprexa), 5 mg, single dose
Arm Title
Haloperidol
Arm Type
Active Comparator
Arm Description
Haloperidol encapsulated tablet, 2 mg tablet, single dose
Arm Title
Diazepam
Arm Type
Active Comparator
Arm Description
Diazepam encapsulated tablet, 2mg tablet, single dose
Intervention Type
Drug
Intervention Name(s)
Olanzapine oro-dispersible 5Mg Tab
Other Intervention Name(s)
Zyprexa
Intervention Description
Patient allocated to this arm will be given 5 mg olanzapine oro-dispersible tablet and an encapsulated placebo tablet
Intervention Type
Drug
Intervention Name(s)
Haloperidol 2Mg encapsulated Tab
Intervention Description
Patient allocated to this arm will be given 2 mg encapsulated haloperidol tablet and an oro-dispersible placebo tablet
Intervention Type
Drug
Intervention Name(s)
Diazepam 2Mg encapsulated Tab
Intervention Description
Patient allocated to this arm will be given 2 mg encapsulated diazepam tablet and an oro-dispersible placebo tablet
Primary Outcome Measure Information:
Title
Time to achieve adequate sedation
Description
Adequate sedation is determined by a 6-point validated scale
Time Frame
Within 60 minutes from drug administration
Secondary Outcome Measure Information:
Title
Total study drug doses administered; alternative drugs and doses used
Time Frame
From Accident & Emergency Department(AED) admission to transfer or discharge from AED, an expected average of 1 hour
Title
Corrected QT interval (QTc)
Time Frame
From Accident & Emergency Department(AED) admission to transfer or discharge from AED, an expected average of 1 hour
Title
AED length of stay (LOS)
Time Frame
From Accident & Emergency Department(AED) admission to transfer or discharge from AED, an expected average of 1 hour
Title
Adverse events
Description
including airway management (jaw thrust, oral, nasal airway), need for assisted ventilation (bag/mask, intubation), oxygen desaturation <90%, systolic BP<90 mmHg, dystonic reactions, seizures, vomiting or aspiration
Time Frame
From Accident & Emergency Department(AED) admission to transfer or discharge from AED, an expected average of 1 hour

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Accident & Emergency Department patients Requiring oral drug sedation (as determined by an emergency clinician) will be enrolled. Exclusion Criteria: known hypersensitivity or contraindication to the study drugs reversible aetiology for agitation (e.g. hypotension, hypoxia, hypoglycaemia) known pregnancy acute alcohol withdrawal refusal to take oral medication patients from correctional facilities
Facility Information:
Facility Name
Queen Elizabeth Hospital
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Citations:
PubMed Identifier
16091097
Citation
Knott JC, Bennett D, Rawet J, Taylor DM. Epidemiology of unarmed threats in the emergency department. Emerg Med Australas. 2005 Aug;17(4):351-8. doi: 10.1111/j.1742-6723.2005.00756.x.
Results Reference
background
PubMed Identifier
22981685
Citation
Chan EW, Taylor DM, Knott JC, Phillips GA, Castle DJ, Kong DC. Intravenous droperidol or olanzapine as an adjunct to midazolam for the acutely agitated patient: a multicenter, randomized, double-blind, placebo-controlled clinical trial. Ann Emerg Med. 2013 Jan;61(1):72-81. doi: 10.1016/j.annemergmed.2012.07.118. Epub 2012 Sep 13.
Results Reference
background
PubMed Identifier
16387219
Citation
Knott JC, Taylor DM, Castle DJ. Randomized clinical trial comparing intravenous midazolam and droperidol for sedation of the acutely agitated patient in the emergency department. Ann Emerg Med. 2006 Jan;47(1):61-7. doi: 10.1016/j.annemergmed.2005.07.003. Epub 2005 Aug 18.
Results Reference
background
PubMed Identifier
21091874
Citation
Chan EW, Taylor DM, Knott JC, Kong DC. Variation in the management of hypothetical cases of acute agitation in Australasian emergency departments. Emerg Med Australas. 2011 Feb;23(1):23-32. doi: 10.1111/j.1742-6723.2010.01348.x. Epub 2010 Nov 22.
Results Reference
background
PubMed Identifier
19527287
Citation
Chan EW, Knott JC, Taylor DM, Phillips GA, Kong DC. Intravenous olanzapine--another option for the acutely agitated patient? Emerg Med Australas. 2009 Jun;21(3):241-2. doi: 10.1111/j.1742-6723.2009.01190.x. No abstract available.
Results Reference
background
PubMed Identifier
23186399
Citation
Chan EW, Taylor DM, Knott JC, Liew D, Kong DC. The pharmacoeconomics of managing acute agitation in the emergency department: what do we know and how do we approach it? Expert Rev Pharmacoecon Outcomes Res. 2012 Oct;12(5):589-95. doi: 10.1586/erp.12.53.
Results Reference
background
PubMed Identifier
26635127
Citation
Chan EW, Tang C, Lao KS, Ling Pong L, Tsui MS, Ho HF, Wong GC, Kong DC, McD Taylor D, Knott JC, Wong IC. Management of acute agitation in Hong Kong and comparisons with Australasia. Emerg Med Australas. 2015 Dec;27(6):542-548. doi: 10.1111/1742-6723.12499. Epub 2015 Dec 3.
Results Reference
background
PubMed Identifier
28160494
Citation
Yap CYL, Taylor DM, Knott JC, Taylor SE, Phillips GA, Karro J, Chan EW, Kong DCM, Castle DJ. Intravenous midazolam-droperidol combination, droperidol or olanzapine monotherapy for methamphetamine-related acute agitation: subgroup analysis of a randomized controlled trial. Addiction. 2017 Jul;112(7):1262-1269. doi: 10.1111/add.13780. Epub 2017 Feb 28.
Results Reference
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Oral Olanzapine Versus Haloperidol or Diazepam

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