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Effect of oral magnesium sachet versus placebo on shivering after cesarean section under spinal anesthesia

Effect of oral magnesium sachet versus placebo on shivering after cesarean section under spinal anesthesia: a double-blind randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120215009014N374
Enrollment
50
Registered
2020-12-31
Start date
2021-01-14
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Shivering. Tremor, unspecified

Interventions

Intervention 1: Intervention group: Oral magnesium sachet 300 mg (manufactured by Perarin Pars Co.) single dose half an hour before surgeryRoutine treatment plus. Intervention 2: Control group: Oral p

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age of 18 to 40 years, Women candidate for elective cesarean section,

Exclusion criteria

Exclusion criteria: Temperature less than 36.5 or greater than 38 centigrade, Duration of surgery longer than 180 minutes

Design outcomes

Primary

MeasureTime frame
Shivering. Timepoint: Every 15 minutes immediately after spinal anesthesia until the presence of the patient in the recovery room. Method of measurement: By using a Bedside Four-Point Scale.

Secondary

MeasureTime frame
Nausea and vomiting. Timepoint: During the presence of the patient in the recovery room. Method of measurement: By taking history and clinical observation.;Hypotension. Timepoint: Every 15 minutes immediately after spinal anesthesia until the presence of the patient in the recovery room. Method of measurement: By using sphygmometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYeganeh Sangian

Hamedan University of Medical Sciences

yeganeh.sangian@yahoo.com+98 81 3838 0572

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026