To assess the efficacy of a block to reduce postoperative pain in breast cancer patients
Not Applicable
Completed
- Conditions
- Health Condition 1: - Health Condition 2: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2019/08/020897
- Lead Sponsor
- Govt T D Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age group between 25-70 years posted for radical mastectomy
2. ASA 1-4 patients
Exclusion Criteria
1.Current or historical evidence of clinically significant medical disease or condition 2.History of allergy to local anaesthetics 3.Refusal of patient to participate in study 4.Psychiatric patients 5.BMI >40
6. Patients with preexisting coagulation abnormalities
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method