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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UNKNOWN
NA
200 participants
INTERVENTIONAL
2022-08-25
2023-12-30
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
DOUBLE
Study Groups
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Eto 0.15mg/kg
Etomidate 0.15mg/kg for anesthesia induction
etomidate
use etomidate for anesthesia induction in hysteroscopic surgery
Eto 0.2mg/kg
Etomidate 0.2mg/kg for anesthesia induction
etomidate
use etomidate for anesthesia induction in hysteroscopic surgery
Eto 0.25mg/kg
Etomidate 0.25mg/kg for anesthesia induction
etomidate
use etomidate for anesthesia induction in hysteroscopic surgery
Propofol 2mg/kg
propofol 2mg/kg for anesthesia induction
propofol
use propofol for anesthesia induction in hysteroscopic surgery
Interventions
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etomidate
use etomidate for anesthesia induction in hysteroscopic surgery
propofol
use propofol for anesthesia induction in hysteroscopic surgery
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
60 Years
FEMALE
Yes
Sponsors
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Peking University Third Hospital
OTHER
Responsible Party
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Other Identifiers
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89476
Identifier Type: -
Identifier Source: org_study_id
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