comparison of two blocks for pain relief in modified radical mastectomy
Phase 2
- Conditions
- Health Condition 1: C508- Malignant neoplasm of overlappingsites of breast
- Registration Number
- CTRI/2019/09/021030
- Lead Sponsor
- PGIMER Dr RML Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All female patients in the age group of 18-80 years scheduled to undergo modified radical mastectomy under general anesthesia
Exclusion Criteria
Local infection at the block site, coagulopathy, allergic to local anesthetic, bleading disorders, pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of first rescue analgesic requirementTimepoint: time of administration of block and the time patient complaints of pain
- Secondary Outcome Measures
Name Time Method Average Visual Analog Score in 12hrs, total rescue analgesic requirement in 12hrs, intraoperative and postoperative hemodynamic changes, complicationsTimepoint: 30 minutes, 2nd hour, 4th hour, 8th hour and 12th hour