Comparison Between Propofol-remifentanil Total Intravenous Anesthesia and Desflurane-remifentanil Balanced Anesthesia With Regard to Post-anesthetic Functional Recovery Measured With QoR-40 in Vitrectomy
NCT ID: NCT02212340
Last Updated: 2016-09-27
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
84 participants
INTERVENTIONAL
2014-07-31
2016-03-31
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
PREVENTION
DOUBLE
Study Groups
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TIVA group
Anesthesia is maintained with fresofol and remifentanil
fresofol and remifentanil
Anesthesia is maintained with fresofol and remifentanil in TIVA group or with desflurane and remifentanil in Des group according to randomly allocated group.
Des group
Anesthesia is maintained with desflurane and remifentanil
desflurane and remifentanil
Anesthesia is maintained with fresofol and remifentanil in TIVA group or with desflurane and remifentanil in Des group according to randomly allocated group.
Interventions
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fresofol and remifentanil
Anesthesia is maintained with fresofol and remifentanil in TIVA group or with desflurane and remifentanil in Des group according to randomly allocated group.
desflurane and remifentanil
Anesthesia is maintained with fresofol and remifentanil in TIVA group or with desflurane and remifentanil in Des group according to randomly allocated group.
Eligibility Criteria
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Inclusion Criteria
2. ASA 1-3
Exclusion Criteria
2. Anticipated difficult airway
3. BMI \> 30 kg/m2
4. Chronic obstructive pulmonary disease
5. Heart failure 6. Unstable angina
20 Years
80 Years
ALL
No
Sponsors
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Yonsei University
OTHER
Responsible Party
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Locations
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Gangnam Severance Hospital, Yonsei University College of Medicine
Seoul, Seoul, South Korea
Countries
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Other Identifiers
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3-2014-0104
Identifier Type: -
Identifier Source: org_study_id
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