Comparison of two drugs given along with local anaesthetic in an ultrasound guided procedure for pain relief in breast surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/04/051761
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients belonging to ASA physical status I and II posted for oncological breast surgery with or without reconstruction with at least 24 hours hospital stay
Exclusion Criteria
1. patient refusal
2. patients with any containdications to regional anaesthesia such as coagulopathy or local infection at the site of injection
3. patients with history of anaphylaxis to local anaesthetics and allergy to study drugs
4. patients with history of underlying psychological disorder
5. patients with chronic systemic illness
6. patients with bleeding diathesis
7. pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method duration of analgesiaTimepoint: from the time of injection of drug in SAP block to the request for first rescue analgesia in PACU till 24 hours
- Secondary Outcome Measures
Name Time Method 1. VAS <br/ ><br>2. total postoperative opioid consumptionTimepoint: 1. at PACU,at 2,4,6,8,12,16,20,24 hours <br/ ><br>2. at 24 hours postop.