Subcutaneous infiltration of local anesthetic for postoperative pain following breast surgery
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: - Health Condition 3: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2024/07/070960
- Lead Sponsor
- amratha.M
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)ASA Grade 1,2
2)Age between 30-70 years
3)Female patients undergoing breast surgery
Exclusion Criteria
1)Patient Refusal
2) ASA III and above
3) Patient with Coagulation disorders or on anticoagulant and antiplatelet drugs
4) Infection at the site of injection
5) Known allergy to the any of study drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate efficacy of portal blocks for post-operative pain management in woman undergoing Breast surgeryTimepoint: 20minutes after block, followed by every 2 hourly upto 48 hours
- Secondary Outcome Measures
Name Time Method To Evaluate patient satisfaction & effects on hemodynamic parametersTimepoint: starting from 20 minutes after the block, followed by every 2 hours for 48hours post surgery