Effect of Dexmedetomidine on Bispectral Index and Propofol Requirements During Different Menstrual Cycle
NCT ID: NCT02035930
Last Updated: 2014-01-14
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
PHASE4
110 participants
INTERVENTIONAL
2010-11-30
2012-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
DOUBLE
Study Groups
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menstrual cycle,dexmedetomidine
dexmedetomidine
Interventions
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dexmedetomidine
Eligibility Criteria
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Inclusion Criteria
* elective gynecologic surgery
Exclusion Criteria
* breastfeeding
* obesity
* known hypersensitivity to drugs used in the study protocol;
* use of psychotropic drugs and steroids within 72 hours before the surgery
* central nervous system injury
* renal impairment
* alcoholism and opioid addiction.
24 Years
40 Years
FEMALE
No
Sponsors
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Fudan University
OTHER
Responsible Party
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Geng guiqi
professor
Other Identifiers
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TWang
Identifier Type: -
Identifier Source: org_study_id
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