Comparison of two pain reducing techniques after breast cancer surgery.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients with breast cancer
- Registration Number
- CTRI/2018/04/012915
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
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.Patient refusal
2.Age <18 or > 70 years
3.Patients with BMI > 35kg/m2
4.Patient with infection at the site of injection
5.Coagulopathy
6.Spine deformity
7.Drug addicts or history of opioid dependence
8.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 analgesia (that is, time to first analgesic request from the time of giving block ). <br/ ><br>Timepoint: Pain assessment would be done in immediate post (0 min), 30 min, 1 hr , 2hr , 6hr, 12 and 24 hr.
- Secondary Outcome Measures
Name Time Method 1) Total rescue analgesic requirement in postoperative period. <br/ ><br>2) To evaluate patient satisfaction in postoperative period. <br/ ><br>Timepoint: Patient satisfaction would be evaluated at 24 hrs after surgery