se of Costoclavicular block in Frozen shoulder syndrome to produce analgesia
Phase 4
- Conditions
- Health Condition 1: - Health Condition 2: M750- Adhesive capsulitis of shoulderHealth Condition 3: M256- Stiffness of joint, not elsewhereclassified
- Registration Number
- CTRI/2022/02/040397
- Lead Sponsor
- Sancheti institute for orthopaedics and rehabilitation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other (Terminated)
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
BMI <25
Exclusion Criteria
Patient with MRI noncompatible implant,
history of surgery of ipsilateral clavicle/ shoulder,
history of MRI contrast/ local anaesthetic drug allergy
COPD, PREGNANCY,Contralateral Phrenic nerve paresis, diabetes mellitus
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - To evaluate analgesic efficacy of costoclavicular block. Adequate analgesia will help patient to perform shoulder rehabilitation exercises efficiently.Timepoint: Post injection patient will be monitored in recovery room for vital signs every 10min for 1hr. <br/ ><br>Patients SPADI score will be evaluated at 1st hr by shoulder surgery resident. <br/ ><br> Two hours later SPADI will be reassessed and post block 50% reduc-tion in shoulder pain will be taken as positive response. A clinical score would be assigned to patient. <br/ ><br>After surgeon finishes clinical assessment, patient will be shifted to scan area for performing ipsilateral shoulder & neck MRI scan.
- Secondary Outcome Measures
Name Time Method To understand the spread of contrast with help of MRI images after costocla-vicular block <br/ ><br> - To assess incidence of hemidiaphragmatic paresis. <br/ ><br>Timepoint: 2hr