At a glance
ClinicalIndex Comparison RecordN/ACompleted· 50 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in 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.
Evaluation of High and Low Flow Sevoflurane Anesthesia in Pediatric Patients Undergoing Laparoscopic Surgeries in Terms of Recovery, Hemodynamics, and Cost
In Brief
An observational study for Low-flow Anesthesia. Completed, enrolled 50 participants across 2 sites.
Detailed Summary
The primary objective of our study is to compare the effects of different flow rates of the routinely used inhalation agent, sevoflurane, on postoperative recovery times in pediatric patients undergoing elective laparoscopic surgeries. Our secondary objectives are to evaluate the impact of different flow rates on hemodynamic parameters, ventilation parameters, and costs.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsLow-flow Anesthesia
CountriesTurkey (Türkiye)
Collaborators--
Timeline
N/ACompletedFinished
20252026
Enrollment StartMay 2024
Primary CompletionSep 2024
Study CompletionOct 2024
First PostedNov 2024
TodayJul 2026
First PostedNov 6, 2024
Enrollment StartMay 1, 2024
Primary CompletionSep 30, 2024
Study CompletionOct 7, 2024
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 1.7 years ago