To compare the efficacy of two types of anesthesia techniques on post operative pain relief in patients undergoing breast cancer study
Not Applicable
Completed
- Registration Number
- CTRI/2019/08/020865
- Lead Sponsor
- Dr BRA IRCH AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
1. Age 18-7O years
2. ASA I and II
3. Patients posted for breast cancer surgery
4. Patients giving written informed consent to participate in the study
Exclusion Criteria
1. Patient refusal
3. Patients with BMI > 35kg/m2
4. Patient with infection at the site of injection
5. Coagulopathy
6. Spine deformity
7. Drug addicts or history of opioid dependence
8. Patients with history of allergy to opioids,local anaesthetics or magnesium.
9. Patients with myopathy or neuropathy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Analgesic efficacy in terms of total postoperative morphine consumption in 24 hoursTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method eutrophil-Lymphocyte ratio (NLR), Platelet Lymphocyte Ratio (PLR) and number of Natural Killer Cells (NKCs), T helper cells, cytotoxic T cellsTimepoint: 1 day prior to surgery, immediate post operative period, 24 hours post operatively;NRS pain scoreTimepoint: 0,30 min, 1hr. 2hr, 6hr, 24hr post operatively.;Patient satisfaction in a likert scale of 1-7Timepoint: 24 hours post operatively;Side effects if anyTimepoint: 0, 30 min, 1 hr, 2 hr, 6 hr, 24 hr post operatively