To see pain relief after analgesic injections in chest wall muscle layers in patients undergoing breast surgery.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Breast cancer
- Registration Number
- CTRI/2017/10/009965
- Lead Sponsor
- Sanjay Gandhi Post Graduate Institute Of Medical Sciences Lucknow
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 66
Inclusion Criteria
Patients undergoing modified radical mastectomy.
Exclusion Criteria
1)pregnant females
2)patients allergic to local anaesthetics
3)patients undergoing mastectomy with reconstruction
4)age < 18yrs / > 60yrs
5)patient with other comorbidities
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method dynamic and static pain using visual analogue scale (VAS) <br/ ><br>Timepoint: immediate postop <br/ ><br>postop 12hrs <br/ ><br>24 hrs <br/ ><br>48hrs <br/ ><br>1mth <br/ ><br>3mths <br/ ><br>6mths <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1)shoulder pain (VAS) and function by range of motion (ROM) <br/ ><br>2)duration of analgesia, <br/ ><br>3)pain disability index (PDI) <br/ ><br>4)other side effects eg sedation, hemodynamics, postoperative nausea and vomiting. <br/ ><br> <br/ ><br>Timepoint: shoulder pain and ROM <br/ ><br>immediate postop <br/ ><br>postop 12hrs <br/ ><br>24 hrs <br/ ><br>48hrs <br/ ><br>1mth <br/ ><br>3mths <br/ ><br>6mths <br/ ><br>