Evaluation of effect of the local infltration of bupivacain with or without dexamethasone on severity of acute pain in women undergoing cesarian sectio
Phase 3
Recruiting
- Conditions
- Pain from cesarean section.Pelvic and perineal painR10.2
- Registration Number
- IRCT20220501054713N1
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 75
Inclusion Criteria
1- Pregnant women in the age range of 18 to 40 years
2- Women who are in ASA1 and ASA2 groups according to ASA (American Society of Anesthesiologists) in terms of physical condition.
Exclusion Criteria
Long surgery longer than two hours
History of allergy to local anesthetics
History of cesarean section more than twice
History of drug abuse
History of fibromyalgia or chronic nerve pain
BMI above 35
Change the type of surgery.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analogue Scale Score after cesarean section. Timepoint: VAS score after cesarean section at zero hours of recovery and one hour after surgery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Dosage of the drug in the first 24 hours after cesarean section. Timepoint: the first 24 hours after cesarean section. Method of measurement: Total dose of drugs used per mg/dl.