We compare continuous infusion and intermittent bolus infusion post operative patient-controlled analgesia with erector spinae block catheter
Not Applicable
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2021/05/033759
- Lead Sponsor
- AIIMS Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I/II female patients scheduled for unilateral MRM under general anaesthesia
Exclusion Criteria
Patients unable to cooperate or give consent
Known allergy to local anesthetic, non-steroidal anti-inflammatory drugs or opioids,
Infection at the injection site,
Coagulopathy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assess the consumption of local anesthetic during PCA in 24 hoursTimepoint: 24 hour
- Secondary Outcome Measures
Name Time Method 1.Numerical rating scores (NRS) <br/ ><br>2.the frequency of PCA use <br/ ><br>3.patient satisfaction <br/ ><br>4. side effects <br/ ><br>Timepoint: 24 hours