Effects of Volatile and Intravenous Anesthetics on Pupillary Function
NCT ID: NCT03987529
Last Updated: 2020-08-17
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
22 participants
OBSERVATIONAL
2020-08-12
2021-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Sevoflurane+Remifentanil
Using inhalent agent(Sevoflurane), continuous infusion of Remifentanil
sevoflurane
volatile anesthetic
Propofol+Remifentanil
Using continuous infusion of Propofol and Remifentanil
propofol
intravenous anesthetic
Interventions
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sevoflurane
volatile anesthetic
propofol
intravenous anesthetic
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Any severe side effects, adverse drug reaction
3 Years
12 Years
ALL
No
Sponsors
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Seoul National University Hospital
OTHER
Responsible Party
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Hee-Soo Kim
professor
Principal Investigators
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Hee-Soo Kim, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Seoul National University Hospital
Locations
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Seoul National University Hospital
Seoul, , South Korea
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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H1906-096-1040
Identifier Type: -
Identifier Source: org_study_id
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