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DSIP

Emideltide, DSIP nonapeptide, Delta sleep-inducing peptide

Quick Stats
Studies 458
Trials 82
Completed PHASE3 INTERVENTIONAL NCT03022240

Neurobiological and Cognitive Changes Following Exposure to Either Sevoflurane- or Propofol-based Anesthesia in Children

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The demand for magnetic resonance imaging (MRI) in pediatric patients is increasing due to its use in medical diagnosis and surveillance. Pediatric patients often require general anesthesia (GA) for MRI due to the need for prolonged immobility during the scanning process to obtain high quality images. Two widely used anesthetic techniques for pediatric MRIs are volatile-based anesthesia using sevoflurane and total intravenous anesthesia (TIVA) using propofol. Concerns have been raised regarding the potential neurotoxic effects of anesthetics on the developing brain. Within the animal literature, there is emerging evidence to suggest that both sevoflurane and propofol may cause inflammation, impacting brain cell survival and connections, thereby contributing to possible cognitive dysfunction. However, given the challenges in extrapolating the animal data to humans, and the relatively limited human cohort studies examining the long-term effects of anesthesia exposure, there is inadequate information available to make informed clinical decisions regarding the choice of optimal anesthetic agents for MRI in children. Therefore, this study will uniquely examine the mechanisms of two widely used anesthetics and their short and long-term impact on developmental outcomes in healthy children.

Interventions

Name: Propofol
Type: DRUG
Description: The child will be randomized via a block design to receive either a volatile anesthetic (induction: sevoflurane), or total intravenous anesthetic technique (induction: propofol)
Name: Sevoflurane
Type: DRUG
Description: The child will be randomized via a block design to receive either a volatile anesthetic (induction: sevoflurane), or total intravenous anesthetic technique (induction: propofol)
Name: Ametop
Type: DRUG
Description: Each patient will receive Ametop local anesthetic to the dorsum of both hands 30-45 minutes prior to induction.
Name: Ondansetron
Type: DRUG
Description: Each patient will receive the antiemetic ondansetron 0.1mg/kg IV.

Primary Outcomes

Measure: Wechsler Preschool and Primary Scale of Intelligence (WPPSI-IV)
TimeFrame: 12-15 weeks from date of randomization
Description: The WPPSI - IV is designed for children aged 2.5 to 7.5 years, and is used to assess general intelligence.

Trial Information

NCT ID

NCT03022240

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE3

Sponsor

University of Calgary

Last Updated

December 15, 2025