It is a study to see the effectiveness of Erector Spinae Plane Block in patients presenting with complain of recurring shoulder pai
Not Applicable
Completed
- Conditions
- Health Condition 1: -
- Registration Number
- CTRI/2021/04/032684
- Lead Sponsor
- Department of anaesthesiology and critical care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Patients of either sex, between 40-70 year of age, with chronic shoulder pain of duration more than six months not responding to at least two weeks of analgesics and conservative therapy, referred to pain clinic will be enrolled in the study
Exclusion Criteria
Patient with known contraindication for block interventions (e.g. infection at site of block, coagulopathy),history of adverse reaction to steroids and bupivacaine, uncontrolled diabtes mellitus and patients not consenting for erector spinae plane block will not be included in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain relieveTimepoint: Pain will be assessed using visual analog scale (VAS 0-10).It will be recorded at the following interval: before the procedure, thirty minutes, one week and four weeks after the block
- Secondary Outcome Measures
Name Time Method DisabilityTimepoint: disability score will be assessed by using SPADI(Shoulder Pain And Disability Index). It will be recorded at the following interval: before the procedure, thirty minutes, one week and four weeks after the block.;Range of motionTimepoint: range of motion will be recorded using goniometer.It will be recorded at the following interval: before the procedure, thirty minutes, one week and four weeks after the block