comparison between erector spinae and paravertebral block for post operative pain in patients undergoing breast surgeries
Not Applicable
- Conditions
- Health Condition 1: C00-D49- Neoplasms
- Registration Number
- CTRI/2024/08/072372
- Lead Sponsor
- DR SWATHI S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patient wiiling to give informed written consent
ASA 1 and ASA 2
Exclusion Criteria
Patient not willing to give informed written consent
Heart block more than 1st degree
pregnancy and lactation
Coagulation disorders
Body Mass Index more than 35kg/m2
Patients who have known allergy to local anesthetics
Heart block greater than 1st degree
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the postoperative pain score using Numerical Rating Scale at 12 hoursTimepoint: To compare the postoperative pain score using Numerical Rating Scale at 12 hours
- Secondary Outcome Measures
Name Time Method 1.The time to first analgesic request <br/ ><br>2.To compare the overall consumption of opiod{Nalbuphine} in 24 hoursTimepoint: 24 hours