Comparison of local anesthesia nerve blocks in breast cancer surgery patients
Not Applicable
- Conditions
- Health Condition 1: C50-C50- Malignant neoplasms of breast
- Registration Number
- CTRI/2023/02/049911
- Lead Sponsor
- All India Institute of Medical Sciences, Raipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Female patients aged 18 years and above, willing to give consent
Belonging to American society of Anaesthesiologists (ASA) grade I, ll & III
BMI 18.5 -29.5 kg/m2
Exclusion Criteria
Patient refusal,
Inability to properly describe postoperative pain toinvestigators (language barrier),
Contraindications to regional anesthesia (bleeding diathesis,raised PT/INR levels, infection at the site of block and peripheral neuropathy),
Allergy to study drugs mainly Bupivacaine and dexamethasone,
Spine deformity .
Psychiatric patients.
Pregnant and lactating females.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to the first dose of rescue analgesia postoperativley based on Visual Analogue Scale (VAS) score â?¥ 4 at 0h,2h,4h,8h,12h,24h <br/ ><br>Timepoint: Time to the first dose of rescue analgesia postoperativley based on Visual Analogue Scale (VAS) score â?¥ 4 at 0h,2h,4h,8h,12h,24h
- Secondary Outcome Measures
Name Time Method 1. Injection fentanyl consumed intraoperatively <br/ ><br>2.Total dose of analgesics consumed in 24 hours post operativley. <br/ ><br>3. Post operative VAS score at 0h,2h,4h,8h,12h,24h <br/ ><br>4. Adverse / side effects (if any).Timepoint: Post operative VAS score at 0h,2h,4h,8h,12h,24h