Comparison of two types of anaesthesia nerve blocks in breast cancer surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Breast LumpHealth Condition 2: C50- Malignant neoplasm of breast
- Registration Number
- CTRI/2017/02/007897
- Lead Sponsor
- All India Institute of Medical Sciences Bhubaneswar Intramural grant
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 58
Inclusion Criteria
Adult patients undergoing breast surgery ( MRM)
Exclusion Criteria
Allergy to LA agent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality and duration of analgesiaTimepoint: Need for opiate rescue, Duration to first request for (non opiate analgesic), VAS scores for first 24 hours post surgery pain scores will be assessed at 0, 30 min, 1 hr, 2 hr and 2nd hrly thereafter at rest and on arm movement. <br/ ><br>the total amount of analgesic consumed at end of 24 hrs post op will be assessed .
- Secondary Outcome Measures
Name Time Method Complications of Block <br/ ><br>Opioid REquirement <br/ ><br>Quality of life on post operative follow up ( Chronic pain)Timepoint: QOL- 3 months and 6 months post op