Comparison of analgesic efficacy of two regional anaesthetic techniques in breast cancer surgery patients.
Not Applicable
- Conditions
- Health Condition 1: null- Patients with clinical diagnosis of breast carcinoma posted for modified radical mastectomy
- Registration Number
- CTRI/2018/07/014913
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Female patients with carcinoma breast
2. Age group -18-70 years
3. ASA Physical status 1,2,3 scheduled to undergo modified radical mastectomy.
Exclusion Criteria
1.Patients Refusal
2.Patients with infection at the site of SAP or ESPB block
3.Patients with severe chest wall deformity
4.Patients with history suggestive of coagulopathy or receiving any anticoagulants
5.Presence of complications like mental illness, severe heart disease (NYHA classification >=3)
6.Any renal or hepatic disorder before surgery 7.Allergic to any drug being used during the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate and compare the time to first dose of rescue analgesic in the post-operative period in patients undergoing modified radical mastectomy under combined general anaesthesia and serratus anterior plane block with patients undergoing modified radical mastectomy under combined general anaesthesia and erector spinae plane block.Timepoint: To evaluate and compare the time to first dose of rescue analgesic at the time when numerical rating score more than 4 in the post-operative period in patients undergoing modified radical mastectomy under combined general anaesthesia and serratus anterior plane block with patients undergoing modified radical mastectomy under combined general anaesthesia and erector spinae plane block.
- Secondary Outcome Measures
Name Time Method a.To evaluate and compare the total dose of rescue analgesic needed intraoperatively. <br/ ><br>b. To evaluate and compare the total dose of rescue analgesics required postoperatively. <br/ ><br>c. To evaluate and compare the patient satisfaction score postoperatively. <br/ ><br> <br/ ><br>Timepoint: The total intraoperative and postoperative analgesics and patients satisfaction scores will be noted till 24 hours after the surgery.