The Effect of Intrathecal Betamethasone on Post Operative Pain Relief after Cesarean Section.
Phase 1
- Conditions
- post operative pain.Acute pain
- Registration Number
- IRCT201012115363N1
- Lead Sponsor
- Vice- Chancellor for Research of Zanjan University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 99
Inclusion Criteria
ASA class I and II, age between 20 and 40 years old, scheduled to undergo Cesarean Section
Exclusion criteria: Receiving analgesics or corticosteroids drugs, presence of contraindication to regional anesthesia, known hypersensitivity to the study drugs or if having any history of cardiac, respiratory, neuromuscular, Hepatic or renal disease, unwilling to participate
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain. Timepoint: 4, 6, 12, 24 h after operation. Method of measurement: VAS-consisting of 100 mm line with 0 = no pain and 100 = worst possible pain.
- Secondary Outcome Measures
Name Time Method umber of used suppository. Timepoint: 24 hrs after surgery. Method of measurement: Asking from Patient.;Nausea and vomiting intraoperatively. Timepoint: At the end of the surgery. Method of measurement: Asking from Patient.;Nausea and vomiting postoperatively. Timepoint: 24 hrs after surgery. Method of measurement: Asking from Patient.;Headache after surgery. Timepoint: 24 hrs after surgery. Method of measurement: Asking from Patient.;Time to rescue analgesic drug for the first time. Timepoint: Whenever the VAS goes higher than 4. Method of measurement: Asking from Patient.