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NCT06676969

High vs. Low Flow Sevoflurane Anesthesia in Pediatric Laparoscopic Surgery: Recovery, Hemodynamics, and Cost Comparison

Completed Last updated 24 January 2025
What this trial tests

trial in Low-flow Anesthesia in 50 participants. Completed in 7 October 2024.

Timeline
1 May 2024
Primary endpoint
30 September 2024
7 October 2024

Quick facts

Lead sponsorOndokuz Mayıs University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment50
Start date1 May 2024
Primary completion30 September 2024
Estimated completion7 October 2024
Sites2 locations across Turkey (Türkiye)

Conditions studied

Sponsor

Ondokuz Mayıs University

Who can join

Adults 1 Month to 12, any sex, with Low-flow Anesthesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Ondokuz Mayıs University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06676969.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing