Incidence of Postthoracotomy Pain Following General Anesthesia: A Comparison Between TIVA and Inhalation Anesthesia
NCT ID: NCT00935571
Last Updated: 2009-07-09
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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UNKNOWN
400 participants
OBSERVATIONAL
2007-10-31
2009-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Group I, Group II
Group I: anesthetized with TIVA (Propofol + Remifentanil)
Group II: anesthetized with inhalation (sevoflurane)
propofol, remifentanil, sevoflurane
Propofol: using target controlled infusion (TCI); 1-3ug/ml remifentanil: using TCI by 5-20 ng/ml sevoflurane: 2-3volume% (1-2 MAC)
Interventions
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propofol, remifentanil, sevoflurane
Propofol: using target controlled infusion (TCI); 1-3ug/ml remifentanil: using TCI by 5-20 ng/ml sevoflurane: 2-3volume% (1-2 MAC)
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Asan Medical Center
OTHER
Responsible Party
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Asan Medical Center
Principal Investigators
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In Cheol Choi, MD, PhD
Role: STUDY_CHAIR
Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine
Locations
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Department of Anesthesiology and Pain Medicine, University of Ulsan College of Medicine, Asan Medical Center
Seoul, , South Korea
Countries
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References
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Gotoda Y, Kambara N, Sakai T, Kishi Y, Kodama K, Koyama T. The morbidity, time course and predictive factors for persistent post-thoracotomy pain. Eur J Pain. 2001;5(1):89-96. doi: 10.1053/eujp.2001.0225.
Other Identifiers
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20090708
Identifier Type: -
Identifier Source: org_study_id
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