UMIN ID: UMIN000001039
Registered date:18/02/2008
A randomized placebo-controlled study of small dose and short duration Haloperidol prophylaxis for elderly at risk for postoperative delirium.
Basic Information
Recruitment status | |
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Health condition(s) or Problem(s) studied | postoperative delirium |
Date of first enrollment | 2007/12/01 |
Target sample size | 120 |
Countries of recruitment | Japan |
Study type | Interventional |
Intervention(s) | Haloperidol 2.5mg will administrated with drip infusion for 3 days after operation in the intervention group. No treatment will be applied to the control group. No treatment will be applied to the control group. |
Outcome(s)
Primary Outcome | Behavioral and psychological disorders assessed with NEECHAM score will purchased from preoperative day to 7 days after operation consecutively. |
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Secondary Outcome |
Key inclusion & exclusion criteria
Age minimum | 75years-old |
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Age maximum | Not applicable |
Gender | Male and Female |
Include criteria | |
Exclude criteria | Emergency surgery. Case of having done treatment intervention on the 0th day (that day of operation) of after the operation. |
Related Information
Primary Sponsor | National Hospital for Geriatrics Medicine |
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Secondary Sponsor | |
Source(s) of Monetary Support | Ministry of Health, Labour and Welfare |
Secondary ID(s) |
Contact
public contact | |
Name | Hideyuki Hattori |
Address | Gengo 36-3, Morioka, Obu city, Aichi Japan |
Telephone | 0562-46-2311 |
Affiliation | National Hospital for Geriatrics Medicine Department of Psychiatry |
scientific contact | |
Name | Junichi Kamiya |
Address | Ibohara 500-1, Jousui, Toyota city, Aichi Japan |
Telephone | 0565-31-1511 |
Affiliation | Aichiken-Kouseiren-Toyota-Kousei Hospital department of surgery |