A study to compare the duration of post operative pain relief after administration of ultrasound-guided Quadratus Lumborum block and Transversus Abdominis Plane block in patients undergoing Cesarean Section.
Not Applicable
- Conditions
- Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
- Registration Number
- CTRI/2024/02/062925
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for Lower Segment Cesarean Section under spinal anaesthesia
Exclusion Criteria
1. ASA physical status III and IV
2. Known allergy to local anaesthetic drugs
3. Coagulation disorders
4. Local infection at the site of block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of postoperative analgesia (time at which first rescue analgesic required)Timepoint: time at which first rescue analgesic required, that is, Numeric Rating Score more than 4
- Secondary Outcome Measures
Name Time Method Adverse effects related to the block- Local hematoma or infection, lower limb weakness, hemodynamic variations .Timepoint: 24 hrs;Maternal satisfactionTimepoint: 24 hrs;Time taken for administration of block (time taken from insertion of needle to administration of drug)Timepoint: time taken from insertion of needle to administration of drug;Total dose of rescue analgesic required in first 24hrs postoperativelyTimepoint: 24 hrs