Comparing Pain Relief Techniques After Arthroscopic Shoulder Surgery: A comparative study
Not Applicable
- Conditions
- Health Condition 1: M859- Disorder of bone density and structure, unspecified
- Registration Number
- CTRI/2024/01/061518
- Lead Sponsor
- Dr Sneha Shashikumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adults above the age of 18 years
ASA I II and III patients
All elective Shoulder arthroscopic surgeries under General Anaesthesia of 2 to 4 hr duration
Exclusion Criteria
Patients Refusal to participate in the study
Presence of any peripheral sensorineural deficit of the limb to which block will be given
Known allergy to the local anaesthetic drugs
Contraindication to Erector spinae plane block or Peri articular injection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of postoperative pain by Numerical Rating Score (NRS)Timepoint: 3 hours
- Secondary Outcome Measures
Name Time Method 1)Duration of post-operative analgesia after each block <br/ ><br>2)Total number of analgesic doses required in first 24 hours <br/ ><br>3)Side effects if any like nausea vomiting, local anaesthetic systemic toxicity <br/ ><br>Timepoint: for 24 hours after giving block