Comparison of analgesic efficacy of wound infiltration with bupivacaine versus bupivacaine and tramadol for postoperative pain relief in lower segment cesarean section under spinal anesthesia
Not Applicable
- Registration Number
- CTRI/2023/07/055456
- Lead Sponsor
- Dr D Y Patil Medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade I or II fit patients.
1.Pregnant women age between 18 to 35 years undergoing Lower Segment Cesarian Section under spinal anesthesia.
2.Hemodynamically stable patients with all routine investigations within normallimits without any other co- morbidities.
Exclusion Criteria
Severe cardiopulmonary, renal or liver disease
1.Preeclampsia & Eclampsia
2.Allergy to tramadol or bupivacaine
3.Patient refusal
4.Patient with ASA Grade III or > III.
5.Patients with drug allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Observe analgesic Efficacy of Wound Infiltration with Bupivacaine for Postoperative Pain Relief in Lower Segment Caesarean Section under Spinal AnaesthesiaTimepoint: Postoperative at 2 hours,4 hours, 6 hours, 12 hours, 24 hours
- Secondary Outcome Measures
Name Time Method Observe analgesic Efficacy of Wound Infiltration with Bupivacaine plus tramadol for Postoperative Pain Relief in Lower Segment Caesarean Section under Spinal AnaesthesiaTimepoint: Postoperative at 2 hours, 4 hours, 6 hours, 12 hours, 24 hours