Effect of Magnesium Sulphate Pretreatment in Pediatric Abdominal Surgery
NCT ID: NCT05736744
Last Updated: 2025-01-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE2/PHASE3
58 participants
INTERVENTIONAL
2023-06-20
2025-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Cis/atracurium/saline placebo
1. The patients will receive 100 ml saline 0.9% at an infusion rate 5 ml/min-1) administered 20 min. before induction of anesthesia.
2. cisatracurium will be administered for intubation at a dose of 0.15 mg/kg IV and Maintenance at a dose of 0.03 mg/kg IV
Cis-Atracurium
Cis-Atracurium will be administered at 0.1-0.15 mg/kg IV bolus for intubation and maintenance at a dose of 0.03 mg/kg iv on fixed intervals.
Cis-Atracurium/MgSO4
1. The patients will be pretreated with magnesium sulphate infusion (30 mg kg-1, total volume 100 ml, infusion rate 5 ml min-1) 20 min. before induction of anesthesia.
2. Cis-Atracurium will be administered at 0.1-0.15 mg/kg IV bolus for intubation and maintenance at a dose of 0.03 mg/kg iv on fixed intervals.
MgSO4
The patients will be pretreated with magnesium sulphate infusion (30 mg kg-1, total volume 100 ml, infusion rate 5 ml min-1) 20 min. before induction of anesthesia.
Cis-Atracurium
Cis-Atracurium will be administered at 0.1-0.15 mg/kg IV bolus for intubation and maintenance at a dose of 0.03 mg/kg iv on fixed intervals.
Interventions
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MgSO4
The patients will be pretreated with magnesium sulphate infusion (30 mg kg-1, total volume 100 ml, infusion rate 5 ml min-1) 20 min. before induction of anesthesia.
Cis-Atracurium
Cis-Atracurium will be administered at 0.1-0.15 mg/kg IV bolus for intubation and maintenance at a dose of 0.03 mg/kg iv on fixed intervals.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Both genders
3. Children who will be scheduled to undergo elective laparoscopic surgeries.
4. Patients with American Society of Anesthesiologist physical status classification of 1 or 2-
Exclusion Criteria
2. Patients on medications that interfered with muscle activity.
3. Allergy to medications used in this study.
4. Neuro-muscular diseases.
5. Renal or hepatic impairment.
6. Hypermagnesemia (\>2.5 mmol) or hypomagnesemia (\<1.7 mmol).
7. Parental refusal to participate in the study
2 Years
12 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Hala Saad Abdel-Ghaffar
Principal Investigator
Principal Investigators
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Hala Abdel-Ghaffar, MD
Role: PRINCIPAL_INVESTIGATOR
Professor of anesthesia and intensive care, faculty of medicine, Assiut university, Assiut, Egypt.
Locations
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Pediatric hospital, faculty of medicine, Assiut university
Asyut, Assiut Governorate, Egypt
Pediatric hospital
Asyut, Assiut Governorate, Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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04-2022-200028
Identifier Type: -
Identifier Source: org_study_id
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