At a glance
ClinicalIndex Comparison RecordN/ACompleted· 40 enrolled
Drug / intervention
propofol +3 moredrug
Likely dose
propofol 5.0 μgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
International Review Board of Gachon University Gil Hospital
In Brief
A clinical study evaluating propofol, Desflurane, and 2 other interventions for Cerebral Ischemia. Completed, enrolled 40 participants.
Detailed Summary
The investigators hypothesized that both propofol and desflurane would decrease the regional oxygen saturation (rSO2) but propofol is likely to reduce rSO2 more than sevoflurane when patients are raised to the sitting position.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCerebral Ischemia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartMar 2011
Primary CompletionAug 2011
First PostedSep 2011
TodayJul 2026
First PostedSep 20, 2011
Enrollment StartMar 1, 2011
Primary CompletionAug 1, 2011
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 14.8 years ago
Interventions
propofoldrug
anaesthesia was induced with the effect-site concentration of propofol 5.0 μg ml-1 mainly.
Desfluranedrug
anaesthesia was maintained by desflurane 4-7vol%
alfentanildrug
administration of alfentanil 10 μg kg-1 for anesthetic induction
Rocuroniumdrug
administration of rocuronium 0.6 mg kg-1 for anesthetic induction