Effect of intravenous Lidocaine on pain intensity after Cesarean sectio
Phase 2
- Conditions
- pain intensity after Cesarean section.Pelvic and perineal pain
- Registration Number
- IRCT201408114365N17
- Lead Sponsor
- Vice chancellor for research of Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
willingness to enter the study and informed written consent; ASA class 1&2; Elective cesarean surgery; Age between 20 and 35 years.
Exclusion criteria: Unwillingness to continue the study; Known lidocaine sensitivity; surgery time more than 1/5 hours; Midline incision for any reason; Any unusual complication during surgery.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: 2, 4, 6, 12, 24 hour after surgery. Method of measurement: VAS) Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method Patient satisfaction of pain control. Timepoint: During 24 hours after surgery. Method of measurement: Data collecting form.;Nausea and vomiting. Timepoint: During 24 hours after surgery. Method of measurement: Data collecting form.;Used morphine amount. Timepoint: During 24 hours after surgery. Method of measurement: Data collecting form.;Used diclofenac amount. Timepoint: During 24 hours after surgery. Method of measurement: Data collecting form.