Clinical Trials Directory

Trials / Completed

CompletedNCT03132701

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
2 Years – 7 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGMagnesiumMg is administered during anesthesia until 5 minutes before surgery ends
DRUGSalineSame volume of saline is infused until 5 minutes before surgery ends

Timeline

Start date
2017-06-08
Primary completion
2017-12-12
Completion
2017-12-12
First posted
2017-04-28
Last updated
2018-08-02

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03132701. Inclusion in this directory is not an endorsement.