A Study of comparison of postoperative analgesic effects of posterior and lateral quadratus lumborum block
Phase 2
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
1.Patients undergoing elective Caesarean section with ASA 2
2.Age from 24 to 40 years old
3.Weight from 50 to 70 Kg
4.Patient of normal single term pregnancy with gestation age of more 37 weeks
Exclusion Criteria
1.Patients not willing for procedure
2.Emergency LSCS
3.Allergic to local anesthetic agent
4.Patient with ASA 3 and 4
5.Coagulopathies
6.Local infections.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in consumption of postoperative IV analgesic agent between two groups. <br/ ><br>Difference in pain score between two groups measured post operatively using visual analogue pain scaleTimepoint: Reduction in consumption of postoperative IV analgesic agent between two groups after 24 hours. <br/ ><br>Difference in pain score between two groups measured post operatively using visual analogue pain scale after 24 hours.
- Secondary Outcome Measures
Name Time Method Compare the hemodynamic changes, nausea, vomiting, pruritis, urinary retentionTimepoint: Outcome is assessed immediately after surgery and up to 24 hours after surgery