Study to compare the effectiveness of drug given under direct vision and under ultrasound to blunt the pain after breast removal surgery
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/063317
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing unilateral modified radical mastectomy under general anesthesia.
Age group between 18 to 65 years of either gender, giving valid informed and written consent.
American Society of Anaesthesiologist grade I and II
Exclusion Criteria
Patients with any contraindication to regional anesthesia.
Patients with a history of anaphylaxis to local anaesthetics and allergy to the study drugs.
Pregnant or lactating patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method