Oral Versus Intravenous Magnesium on Emergence Delirium
Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age4-7
SponsorTanta University
About this trial
This prospective randomized controlled study will be conducted to compare the effects of preoperative oral magnesium and intraoperative IV magnesium on the incidence and severity of emergence delirium in children undergoing adenotonsillectomy using sevoflurane anesthesia.
Eligibility criteria
Qualifiers
Children aged 4 to 7 years
American Society of Anesthesiologist (ASA) Status I or II
Planned for an adenotonsillectomy procedure under sevoflurane general anesthesia.
Disqualifiers
Parents declined to participate in the trial
Behavioral changes, neurological or psychiatric problems
Anticonvulsant or sedative drugs
Physical or developmental abnormalities
Trial design
Treatments tested in this trial
- Magnesium glycinate
- Magnesium sulfate injection
- Oral juice and intravenous saline
Treatment groups
360 Participants
are divided into 3 treatment groupsLocations
1Tanta University Hospitals31527, TantaGharbia Governorate, Egypt
Sponsors and collaborators
Tanta University
Lead sponsor
Source ClinicalTrials.gov