Comparsion of intraincisional bupivacaine, tramadol and bupivacaine plus tramadol in postoperative pain in elective cesarean section patients
Phase 3
- Conditions
- Cesarean section pain control.Delivery by emergency caesarean sectionO82.1
- Registration Number
- IRCT20110306005993N3
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
Age between 15-45 years
Have informed written consent to cooperate with the study
Patient classification in class ASA1,2
Exclusion Criteria
The patient refused to continue collaborating in this study
Adequate spinal anesthesia and its conversion to general anesthesia
Allergy to any of the drugs used
History of addiction
Existence of underlying pain such as back pain, headache
History of using psychiatric drugs
Get preoperative housing
History of addiction
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of pain. Timepoint: Intervals 6, 12 and 24 hours after surgery. Method of measurement: The Visual Analogue Scale (VAS) consists of a pain ruler that includes a horizontal line that is graded from zero to 10, with a 0-1 sign of pain 2-3 mild pain 4-6 moderate pain and 7 or more It is a sign of severe pain. In addition, it has various visual forms to determine the severity of pain.
- Secondary Outcome Measures
Name Time Method ausea and vomiting. Timepoint: Intervals of 6, 12 and 24 hours. Method of measurement: Yes-no based on patient observations and statements.