Requirement of Propofol for Induction of Unconsciousness in Patients With Parkinson's Disease
NCT ID: NCT01998204
Last Updated: 2013-11-28
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
62 participants
OBSERVATIONAL
2012-01-31
2013-06-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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PD group
Patients with Parkinson's disease undergoing deep brain stimulator implantation and pulse generator placement
No interventions assigned to this group
non-PD group
Patients without Parkinson's disease undergoing intracranial surgery
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* non-Parkinsonian patients without Parkinson's disease undergoing intracranial surgery under general anesthesia
Exclusion Criteria
* predicted difficult airway
* hearing impairment
* inability to corporate with instruction
* alcohol or drug abuser
* patients refusing to provide informed consent
18 Years
ALL
No
Sponsors
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Changhai Hospital
OTHER
Responsible Party
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Jia-feng Wang
Dr.
Principal Investigators
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Jia-feng Wang, M.D.
Role: PRINCIPAL_INVESTIGATOR
Department of Anesthesiology, Changhai Hospital, Second Military Medical University
Locations
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Department of Anesthesiology, Changhai Hospital
Shanghai, Shanghai Municipality, China
Countries
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References
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Xu XP, Yu XY, Wu X, Hu XW, Chen JC, Li JB, Wang JF, Deng XM. Propofol requirement for induction of unconsciousness is reduced in patients with Parkinson's disease: a case control study. Biomed Res Int. 2015;2015:953729. doi: 10.1155/2015/953729. Epub 2015 Oct 1.
Other Identifiers
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Parkinson-propofol
Identifier Type: -
Identifier Source: org_study_id