Study of post operative pain relief by comparing the effect of two nerve blocks given to patients undergoing breast removal surgery.
Not Applicable
Completed
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2019/06/019656
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
Weight > 50 kgs
Exclusion Criteria
Pregnancy, any bleeding disorders, infection at injection site, severe/morbid obesity,allergy to local anaesthetics.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparing efficacy of modified PECS block vs. Erector Spinae block in postop period using NRS score and fentanyl requirement in the first 24 hours.Timepoint: First 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method Requirement of intraop fentanyl, incidence of PONV, Ease of physiotherapy in postop period, Patient satisfaction using 7 point Likert questionnaire, any other complicationsTimepoint: First 24 hours postoperatively