PACTR202310525672884
Not yet recruiting
Phase 4
Analgesic effectiveness of wound infiltration with bupivacaine and a mixture of bupivacaine and tramadol for postoperative pain management among participants undergoing elective cesarean section under spinal anesthesia at Dilla university general hospital, 2023: a double-blind randomized controlled trial
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Fertility-female
- Sponsor
- Dilla University
- Enrollment
- 60
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •?Pregnant mothers between 18 and 45
- •?ASA class \=II
Exclusion Criteria
- •?Patients with known allergies to bupivacaine and tramadol
- •?History of alcohol usage, opiate or other drug abuse
- •?Pregnant mothers who diagnosed with Chronic pain
- •?Pregnant mothers with systemic diseases like renal impairment, chronic liver disease, chronic obstructive pulmonary disease, and cardiac disease
- •?Pregnant mothers with pre\-eclampsia, eclampsia
- •?Spinal anesthesia with adjuvants
- •?Operation other than the lower uterine segment incision
- •?Pregnant mothers taking opioids preoperatively
Outcomes
Primary Outcomes
Not specified
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