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The Effect of Magnesium Supplementation During General Anesthesia on the Quality of Postoperative Recovery in Children

Emergence Delirium Clinical Trial

Official title:
The Effect of Magnesium Supplementation During General Anesthesia on the Quality of Postoperative Recovery in Children

Clinical Trial Summary

Evaluation of prevention of emergence delirium and analgesic effect of magnesium on children

Clinical Trial Description

Children < 8 years old who scheduled for elective opthalmic surgery are randomly assigned to Magnesium (Mg) group and control group. Before anesthetic induction, modified Yale Preoperative Anxiety Scale (m-YPAS) is assessed. Routine anesthetic induction is performed, and neuromuscular blocker is not used. Laryngeal mask airway is inserted and controlled ventilation is started.

In Mg group, Mg of 30 mg/kg is administered for 10 minutes and then continuously infused (10mg/kg/hr) until 5 minutes before surgery end. In control group, the similar volume of saline is infused.

Pediatric Anesthesia Emergence Delirium (PAED) scale and pain score (Modified Children's Hospital of Eastern Ontario Pain Scale, CHEOPS) will be measured immediately after and 30 minutes after surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03132701
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date June 8, 2017
Completion date December 12, 2017
View Details
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