Perioperative Risk Factors for Postoperative Delirium in Children
NCT ID: NCT01032161
Last Updated: 2013-02-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
300 participants
OBSERVATIONAL
2009-12-31
2012-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Delirium
Delirium was determined by RASS-PAEDS
No interventions assigned to this group
no Delirium
no Delirium was determined by RASS-PAEDS
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* elective non-cardiovascular surgery
* general anesthesia
Exclusion Criteria
* instable vital sign
* without consent form
* underwent neurosurgery
* history of primary neurologic diseases
* stayed less than 10min in PACU
* received general anaesthesia but recovered in locations outside the recovery room
3 Years
12 Years
ALL
No
Sponsors
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Huazhong University of Science and Technology
OTHER
Responsible Party
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Wei Mei
Associate Professor
Principal Investigators
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Chuanhan Zhang, M.D.
Role: STUDY_DIRECTOR
Department of Anaesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Yuke Tian, M.D.
Role: STUDY_CHAIR
Department of Anaesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Locations
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Department of Anaesthesiology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China
Countries
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Other Identifiers
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TIHMZK02002
Identifier Type: -
Identifier Source: org_study_id
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