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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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JPRN |
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Last refreshed on:
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17 October 2023 |
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Main ID: |
JPRN-UMIN000002891 |
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Date of registration:
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14/12/2009 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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A study on the prevention of postoperative delirium for the elderly
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Scientific title:
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A study on the prevention of postoperative delirium for the elderly - A study on the prevention of postoperative delirium for the elderly |
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Date of first enrolment:
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2009/12/01 |
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Target sample size:
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120 |
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Recruitment status: |
Complete: follow-up complete |
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URL:
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https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003526 |
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Study type:
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Interventional |
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Study design:
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Parallel Randomized
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Phase:
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Not selected
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Countries of recruitment
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Japan
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Contacts
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Name:
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Shinji Fukata |
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Address:
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Gengo 35, Morioka-cho, Obu-city, Aichi, Japan
Japan |
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Telephone:
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0562-46-2311 |
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Email:
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fukatash@ncgg.go.jp |
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Affiliation:
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National Center for Geriatrics and Gerontology Departmentof Surgery |
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Name:
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Shinji Fukata |
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Address:
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Gengo 35, Morioka-cho, Obu-city, Aichi, Japan
Japan |
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Telephone:
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0562-46-2311 |
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Email:
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fukatash@ncgg.go.jp |
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Affiliation:
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National Center for Geriatrics and Gerontology Departmentof Surgery |
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Key inclusion & exclusion criteria
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Inclusion criteria:
Exclusion criteria: A patient with emergency surgery, or the case that haloperidol treatment intervention is performed on the 0th postoperative day (the day of operation)
Age minimum:
75years-old
Age maximum:
Not applicable
Gender:
Male and Female
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Health Condition(s) or Problem(s) studied
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postoperative delirium
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Intervention(s)
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In the intervention group, Haloperidol 2.5mg intravenous drip infusion will be performed from postoperative day 1 to day 3
Only serial observations will be applied to the control group
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Primary Outcome(s)
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We chase psychological disorders / abnormal behavior assessed with NEECHAM score from preoperative day to postoperative day 7 consecutively
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Source(s) of Monetary Support
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Ministry of Health, Labour and Welfare (Resarch Grant for Longevity Sciences)
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Ethics review
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Status: YES
Approval date:
Contact:
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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