TO compare the effect of technique of pain relief on recurrence of cancer after breast surgery
Not Applicable
- Conditions
- Health Condition 1: C50-C50- Malignant neoplasms of breast
- Registration Number
- CTRI/2020/06/025582
- Lead Sponsor
- ICMR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA physical status III or less
2. Primary breast cancer for unimastectomy/breast
conservation surgery
4. With or without lymph node dissection
5. Women younger than 75 years
Exclusion Criteria
age more than 75 years
ASA status IV or more
Patient refusal
Coagulopathy
Patients with history of allergy to study drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method on-occurrence of breast cancer at the end of 3-yearsTimepoint: Patients will be examined every six months till three years to screen for local and systemic breast cancer recurrence by clinical assessment at the end of 3-years.
- Secondary Outcome Measures
Name Time Method 1. Biochemical recurrence <br/ ><br>2. Persistent postoperative painTimepoint: 1. blood test will be done baseline, after completion of surgery and after 24 hours. <br/ ><br>2. pain will be assessed e (0 min),30 min, 1 hour, 24 hours, 1 month, 6 month and 12 month.