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.


Grant Data
Project 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.
Principal Investigator
Dr Chan, Esther Wai Yin   (Principal Investigator (PI))
Co-Investigator(s)
Dr Lui Chun Tat   (Co-Investigator)
Dr Tsui Matthew Sik Hon   (Co-Investigator)
Professor Wong Ian Chi Kei   (Co-Investigator)
Dr Kong David CM   (Co-Investigator)
Dr Knott Jonathan Charles   (Co-Investigator)
Professor Taylor David   (Co-Investigator)
Dr Chan Kin Ling   (Co-Investigator)
Dr Leung Ling Pong   (Co-Investigator)
Duration
36
Start Date
2016-06-30
Amount
1072525
Conference 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.
Presentation Title
Keywords
Agitation, Diazepam, Haloperidol, Olanzapine, Sedation
Discipline
Clinical Trials
Panel
Biology and Medicine (M)
HKU Project Code
17111615
Grant Type
General Research Fund (GRF)
Funding Year
2015
Status
Completed
Objectives
1 To determine the safety and efficacy of oral olanzapine oro-dispersible tablets (wafer), in comparison with oral conventional drugs (haloperidol or diazepam) in a three-arm comparison for the sedation of acutely agitated patients in AEDs. Specifically, to determine if administration of oral olanzapine: (a)is more effective than oral haloperidol or oral diazepam alone; (b)is safer than comparison arms with respect to adverse events; (c)decreases the amount of redosing required using the same or alternate drugs; or parenteral sedation.