Different Hemostasis According to the Anesthetic Agents
NCT ID: NCT02151305
Last Updated: 2014-05-30
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
NA
66 participants
INTERVENTIONAL
2010-08-31
2012-04-30
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
SUPPORTIVE_CARE
TRIPLE
Study Groups
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Total intravenous anesthesia group
This group received propofol and remifentanil for the maintenance of general anesthesia.
Propofol, remifentanil
Inhalation anesthesia group
This group received sevoflurane for the maintenance of general anesthesia.
Sevoflurane
Interventions
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Propofol, remifentanil
Sevoflurane
Eligibility Criteria
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Inclusion Criteria
* American Society of Anesthesiologist physical status I or II
Exclusion Criteria
* severe anemia
* liver disease
* kidney disease
* taking a medication interfering with hemostasis
20 Years
80 Years
ALL
No
Sponsors
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Seoul National University Bundang Hospital
OTHER
Responsible Party
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Hyo-Seok Na
Pf
Locations
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Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, South Korea
Countries
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Other Identifiers
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ROTEM_anesthesia
Identifier Type: -
Identifier Source: org_study_id