Comparison of efficacy of two different techniques of Ultrasound guided local anesthetic druginjections for postoperative pain relief in radical breast surgeries.
Not Applicable
Completed
- Conditions
- Health Condition 1: C50- Malignant neoplasm of breast
- Registration Number
- CTRI/2021/12/038627
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
1. ASA I and II
2. Patients posted for MRM
3. Patients giving written informed consent to participate in the study
Exclusion Criteria
1. BMI > 35kg/m2
2. Patient with infection at the site of injection
3. Coagulopathy
4. Spine deformity
5. Drug addicts or history of opioid dependence
6. Patients with history of allergy to opioids or local anaesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure the duration of Post-operative <br/ ><br>analgesia (that is, time to first rescue analgesia <br/ ><br>after administration of block ). <br/ ><br>Timepoint: Post-operative (0 <br/ ><br>min) ,30 min ,1, 2 , 6 ,12 and 24 hours or as per patients request within 24hours in postoperative period
- Secondary Outcome Measures
Name Time Method Comparison of Post-operative pain ( using numeric rating scale) and adverse effectsTimepoint: Post-operative (0 <br/ ><br>min) ,30 min ,1, 2 , 6 ,12 and 24 hours;To evaluate and compare patient satisfaction with the block <br/ ><br>procedure and at the end of 24hours in postoperative period.Timepoint: Immediately after the block and at the end of 24hours in postoperative period.;Total rescue analgesic requirement in <br/ ><br>Post-operative period. <br/ ><br>Timepoint: Post-operative (0 <br/ ><br>min) ,30 min ,1, 2 , 6 ,12 and 24 hours or as per patients request within 24hours of surgery