To evaluate analgesic efficacy of various regional anaesthesia techniques in breast cancer surgery
Not Applicable
- Registration Number
- CTRI/2023/01/048917
- Lead Sponsor
- HCG Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Aanaesthesiologist 1-3
Exclusion Criteria
Non consenting
Known allergy to study drugs
Coagulation disorder
Uncontrolled comorbidities
Infection at surgical site
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative pain score with numeric rating scale at different post operative time periods beginning 0 hour till 48 hours after surgery <br/ ><br>Timepoint: Immediate post operative period at 0 hour 2nd hour 6th hour 12th hour 24th hour and 48 hours after surgery
- Secondary Outcome Measures
Name Time Method Total postoperative opioid consumed <br/ ><br>Time to first rescue analgesia (hr) <br/ ><br>Quality of recovery ( QoR 15) <br/ ><br>Patient satisfaction scores. (PSS)Timepoint: Post operative pain score at different time periods till discharge