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
324 participants
INTERVENTIONAL
2020-07-20
2024-03-06
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
Patients receiving the total intravenous anesthesia using propofol
Propofol
The induction and maintenance of anesthesia was performed by total intravenous anesthesia using propofol. In both groups, remifentanil is continuously infused throughout the surgery.
Inhalation group
Patients receiving inhalation anesthesia using desflurane
Desflurane
The induction and maintenance of anesthesia was performed by inhalation anesthesia using desflurane. In both groups, remifentanil is continuously infused throughout the surgery.
Interventions
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Propofol
The induction and maintenance of anesthesia was performed by total intravenous anesthesia using propofol. In both groups, remifentanil is continuously infused throughout the surgery.
Desflurane
The induction and maintenance of anesthesia was performed by inhalation anesthesia using desflurane. In both groups, remifentanil is continuously infused throughout the surgery.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients who have chronic kidney disease over stage 5 (estimated glomerular filtration rate \[eGFR\] \<15 ml/kg/1.73m2) or have regular hemodialysis preoperatively
18 Years
ALL
No
Sponsors
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Seoul National University Hospital
OTHER
Responsible Party
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Hyun-Kyu Yoon
clinical assistant professor
Locations
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Seoul National University Hospital
Seoul, , South Korea
Countries
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Other Identifiers
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Anesthetics_Nx_AKI
Identifier Type: -
Identifier Source: org_study_id