A Comparative Study of Depth of Anesthesia Monitored by Bispectral Index (BIS) Values
NCT ID: NCT01140100
Last Updated: 2010-06-09
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
PHASE2
82 participants
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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propofol-propofol
propofol
thiopental-propofol
thiopental,propofol
Interventions
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propofol
thiopental,propofol
Eligibility Criteria
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Inclusion Criteria
* having ASA I or II
* scheduled for elective cataract surgery under general anesthesia
Exclusion Criteria
* intake of any central nervous system (CNS) stimulants
* intake of CNS depressants
* intake of Tricyclic antidepressants
* known adverse reaction to the study drugs
18 Years
ALL
No
Sponsors
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Shiraz University of Medical Sciences
OTHER
Principal Investigators
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Sina Ghaffaripour, M.D
Role: PRINCIPAL_INVESTIGATOR
Shiraz University of Medical Sciences
Hilda Mahmoudi, M.D
Role: STUDY_DIRECTOR
Shiraz University of Medical Sciences
Locations
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Shiraz University of Medical Sciences
Shiraz, Fars, Iran
Countries
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Other Identifiers
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85-3211
Identifier Type: -
Identifier Source: org_study_id
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