Comparison of pain intensity and intrathecal complications of 50 and 100 µg morphine with very low dose of naloxone in patients undergoing cesarean sectio
Phase 3
Recruiting
- Conditions
- ????? ??? ?? ????? ??????.Other chronic painG89.29
- Registration Number
- IRCT20091219002883N6
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 94
Inclusion Criteria
Age over 18 years
Pregnant women with prior planning for cesarean section without Majo disease
Absence of pregnancy-induced disease such as preeclampsia
Term twin pregnancy (37 to 42 weeks)
First or second pregnancy
Tendency to cesarean delivery by spinal anesthesia
Exclusion Criteria
Dissatisfaction with participating in the study
Any contraindications to anesthesia with spinal technique
History of any idiocyncratic allergy or reaction to opioid drugs
Chronic pain syndrome or regular use of opioids
There is predictable evidence of anomaly in the fetus
Allergy or intolerance to ketorolac, ibuprofen or oxycodone • Body mass index above 40
Failure of spinal anesthesia
Prolongation of operation time
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduce pain. Timepoint: The first 24 hours after cesarean section. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method The rate of nausea. Timepoint: Once every 6 hours for the first 24 hours after surgery. Method of measurement: questionnaire.