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Efficacy of Intraoperative Magnesium Sulphate vs Dexmedetomidine on Emergence Agitation in Pediatric Patients

Efficacy of Intraoperative Magnesium Sulphate vs Dexmedetomidine on Emergence Agitation in Pediatric Patients Under Sevoflurane Anesthesia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06977425
Enrollment
60
Registered
2025-05-18
Start date
2024-04-01
Completion date
2025-02-10
Last updated
2025-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dexmedetomidine, Emergence Agitation, Magnesium Sulphate, Pediatric Patients

Brief summary

This study aimed to compare the effectiveness of intraoperative magnesium sulfate versus dexmedetomidine infusions on emergence agitation that follows anesthesia using sevoflurane immediately and after 30 min in the post-anesthesia care unit (PACU), regarding Pediatric Anesthesia Emergence Delirium Scale (PAED), Richmond agitation sedation scale (RASS), and hemodynamics

Detailed description

Emergence agitation (EA) is a postoperative phenomenon that occurs in children after sevoflurane anesthesia, with an occurrence rate of up to 80%. Dexmedetomidine acts on α-2 adrenergic receptors, producing sedation and hypnosis with anxiolytic effects, without a clinically significant depressive impact on heart rate, blood pressure, and respiratory rate, complementing an earlier study suggesting the possible effective and safe use of dexmedetomidine as a part of anesthesia care to prevent emergence agitation in children. Magnesium sulfate also has been reported to decrease the incidence and severity of Emergence agitation and the need for postoperative rescue doses of analgesia in children, and its use was not associated with increased postoperative side effects or delayed recovery.

Interventions

DRUGMagnesium sulphate

Patients received an initial intravenous loading dose of 30 mg/kg of 10% magnesium sulfate solution over 10 min. This will be followed by a continuous infusion of (10mg/kg/hr) for the entire duration of surgery.

DRUGDexmedetomidine

Patients received dexmedetomidine infusion 0.5 μg/kg over 10 min as a bolus dose, followed by 0.2 μg/kg/h all over the operation.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
4 Years to 8 Years
Healthy volunteers
No

Inclusion criteria

* Age from 4 to 8 years old. * Both sexes. * Patients American Society of Anesthesiologists (ASA) Physical Status I to II. * Duration of surgery: not exceeding two hours

Exclusion criteria

* Legal guardian refusal. * Neurological abnormalities, such as cerebral palsy. * Any physical and/or developmental challenge. * Patients on sedatives, anticonvulsants, or any medications that may alter conscious level in children. * Coexisting renal or cardiovascular diseases.

Design outcomes

Primary

MeasureTime frameDescription
Pediatric Anesthesia Emergence Delirium Scale30 minutes postoperativelyPediatric Anesthesia Emergence Delirium Scale (PAED). The PAED Scale consists of five characteristics that are each scored by using a 5-point Likert scale: * The child makes eye contact with the caregiver * The child is aware of his or her surroundings * The child's actions are purposeful, * The child is restless * The child is inconsolable We set the threshold score for the presence of pediatric emergence delirium using the PAED Scale at a score higher than or equal to 10 based on the sensitivity and specificity reported in the literature.

Secondary

MeasureTime frameDescription
Blood pressure30 minutes postoperativelyBlood pressure will be recorded from the start of injection till 30 minutes postoperatively.
Richmond agitation sedation scale (RASS)30 minutes postoperativelyThe Richmond agitation sedation scale (RASS) assesses five levels of sedation: * (5) unarousable with no response to voice or physical stimulation * (4) deep sedation with no response to voice but movement to physical stimuli * (3) moderate sedation with movement to voice but no eye contact * (2) light sedation and briefly awakens (ie, less than 10 seconds) with eye contact to voice * (1) drowsy (ie, not fully alert) but has sustained (ie, more than 10 seconds) awakening with eye contact to voice
Heart rate30 minutes postoperativelyHeart rate will be recorded from the start of injection till 30 minutes postoperatively.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026