Comparing two techniques of ultrasound guided nerve block for postoperative pain relief in patients for breast surgery.
Phase 4
- Conditions
- Health Condition 1: null- Patients having carcinoma breast undergoing modified radical mastectomy
- Registration Number
- CTRI/2018/05/013660
- Lead Sponsor
- Sir Ganga Ram Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Gender: female patients undergoing elective unilateral MRM surgery.
2. ASA physical status I, II and III
3. Age more than 18 years
Exclusion Criteria
1. Patientâ??s refusal
2. Declining to give written informed consent,
3. History of allergy to the medications used in the study,
4. Contraindications to regional anesthesia (including coagulopathy and local infection),
•Prior breast surgery except for diagnostic biopsies,
• History of treatment for a chronic pain condition and/or psychiatric disorder.
•ASA grade physical status III/IV
•Metabolic disorders (liver and kidney disease)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference in duration of analgesia between three groupsTimepoint: Difference in duration of analgesia between three groups
- Secondary Outcome Measures
Name Time Method Acute postoperative pain relief as assessed by visual analogue scale (VAS)Timepoint: At o, 30, 60, 90,120 minutes postoperatively;Assess difference in postoperative pain scores at 3 and 6 monthsTimepoint: At 3 and 6 months;Intraoperative analgesic consumptionTimepoint: Throughout intraoperative period;Patient satisfactionTimepoint: At 0, 30, 60,90, 120 minutes postoperatively;Postoperative nausea and vomiting (PONV)Timepoint: At 0, 30, 60, 90, 120 minutes postoperatively