IRCT20090525001946N11RecruitingPhase 3
Investigating the effects of magnesium sulfate compared to placebo in controlling pain during the first 24 hours after cesarean delivery with spinal anesthesia in pregnant women, a double-blind study
Rasht University of Medical Sciences0 sites118 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Sponsor
- Enrollment
- 118
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 9 years to 45 years (—)
- Sex
- Female
Inclusion Criteria
- •Cesarean section with spinal anesthesia
- •Placement in class II of anesthesia
- •Being nuli para
- •Acceptable candidate for caesarean section
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
Investigators
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