About this trial
The aim of this study is to compare the efficacy of magnesium sulphate, ondansetron, and dexmedetomidine in managing post-spinal anesthesia shivering. The primary aim is the time to cessation of shivering after drug administration, while secondary aim include hemodynamic parameters (heart rate, blood pressure, SpO₂ ) and the recurrence of shivering
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age from 18 to 45 years.
Both sexes.
American Society of Anesthesiologists physical status I, II
Scheduled for elective lower abdominal or lower limb surgeries under spinal anesthesia
Disqualifiers
Patients with known allergy to study drugs.
Patients with baseline body temperature outside the normal range (36-37.5°C).
History of thermoregulatory disorders, thyroid dysfunction, or neurological diseases.
Patients receive sedatives, antipsychotics, or antidepressants.
Trial design
Parallel
Treatments tested in this trial
Dexmedetomidin
Drug•Group D (Dexmedetomidine Group): 0.5 µg/kg dexmedetomidine diluted in 100 mL of normal saline.
Mg (magnesium sulfate)
Drug50 mg/kg magnesium sulphate diluted in 100 mL of normal saline.
Ondansetron 8 mg
Drug8 mg ondansetron diluted in 100 mL of normal saline.
Treatment groups
Trial outcomes
Primary outcomes
Time to cessation of shivering after drug administration.
Grade 0: No shivering. * Grade 1: Piloerection or peripheral vasoconstriction but no visible shivering. 4 * Grade 2: Muscular activity in only one muscle group. * Grade 3: Muscular activity in more than one muscle group. * Grade 4: Whole-body shivering.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: