Comparison of block effects between heavy and plain ropivacaine in patients undergoing breast surgery under segmental thoracic spinal block
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: C508- Malignant neoplasm of overlappingsites of breast
- Registration Number
- CTRI/2022/12/048040
- Lead Sponsor
- Department of Anaesthesiology, AIIMS Rishikesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Female patients with breast cancer undergoing unilateral modified radical mastectomy with axillary clearance with duration less than 3 hours.
2) Age >20 years
3) ASA grading, I-III
4) BMI- 20-30 kg/m2
Exclusion Criteria
1) Refusing to participate in study.
2) Any contraindications to sub-arachnoid block.
3) Significant cardiovascular/renal/hepatic disease.
4) Hypersensitivity to any of the study drug
5) Breast reconstructive surgery with muscle flap
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time (onset) to achieve sensory loss at T2 level in both the groupsTimepoint: 5,10,15 minutes of spinal anaesthesia
- Secondary Outcome Measures
Name Time Method Intra-operative outcome- Monitoring of Hemodynamics changesTimepoint: From 0 to every 5 minutes till the end of surgery;Post-operative outcome - Post-operative pain score according to NRS scaleTimepoint: At 0/2/6/12/18/24 hours