low and prophylactic doses magnesium sulfate on pain control. Complications of labour and delivery
Conditions
Interventions
Intervention 1: Intervention group: 50 mg/kg of magnesium sulfate in 100 ml of isotonic normal saline solution produced by Pasteur Institute factory and the Iran Injection and Pharmaceutical Products
Sponsors
Rasht University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
9 Years to 45 Years
Inclusion criteria
Inclusion criteria: Cesarean section with spinal anesthesia Placement in class II of anesthesia Being nuli para Acceptable candidate for caesarean section
Exclusion criteria
Exclusion criteria: Magnesium intake 24 hours before surgery History of any surgery Suffering from kidney dysfunction Suffering from heart dysfunction Suffering from Lung dysfunction Suffering from Liver dysfunction Suffering from Myopathy dysfunction Suffering from neuropathy dysfunction Occurrence of severe preeclampsia symptoms Occurrence of eclampsia symptoms Having contraindications for spinal injection such as injection site infection Having contraindications for spinal injection such as coagulation disorders Severe obesity (BMI>30) Treatment with calcium receptor blocking drugs Drug addiction History of long-term use of steroids Allergy to magnesium Multiple pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amount of pain in the abdominal surgery area. Timepoint: In the first 6, 12, 18, and 24 hours. Method of measurement: Pain with scores between zero and ten using a Numeric Pain Rating Scale.;Amount of headache. Timepoint: At 6, 12, 18, and 24 hours on the first day and at 12 o'clock on the second and third day after the operation. Method of measurement: Using the headache scoring scale (Visual Analog Scale) with scores between 0 and 10.;The amount of painkillers used. Timepoint: In the first 6, 12, 18, and 24 hours. Method of measurement: If the postoperative VAS, NRS score is greater than three. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sensory block. Timepoint: 30 seconds before the skin incision and then from the time the skin incision is made until the end of the surgery, every five minutes until the end of the sensory block.?. Method of measurement: Using a short needle (pin prick test) for sensory block.;Motor block. Timepoint: 30 seconds before the skin incision and then from the time the skin incision is made until the end of the surgery, every five minutes until the end of the sensory block. Method of measurement: Evaluation of motor block based on three questions of modified Bromage scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSedighe Bab Eghbal
Rasht University of Medical Sciences
Outcome results
None listed