To find improvement in pain and functional activity in patients with frozen shoulder using either anterior or posterior technique of shoulder joint injection.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/053105
- Lead Sponsor
- Department of Anaesthesiology And Critical Care, Pt. B.D. Sharma PGIMS, Rohtak.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
With chronic
shoulder pain due to adhesive capsulitis (VAS >=4), of duration more than three months not
responding to at least two weeks of oral analgesics and conservative therapy, referred to pain
clinic will be enrolled in this study
Exclusion Criteria
Patients with
1. known contraindications for regional block (e.g., infection at the site of Block,
coagulopathy)
2. history of adverse reactions to steroids and bupivacaine
3. uncontrolled diabetes mellitus
4. refusal to participate in the study
5. infection, trauma, tumor, and severe osteoporosis of shoulder joint
6. the prior intervention of the shoulder joint
will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare ultrasound-guided anterior versus posterior technique of intraarticular <br/ ><br>glenohumeral joint injection with regard to the improvement of visual analogue <br/ ><br>score (VAS). <br/ ><br>Timepoint: Pain and ROM will be recorded before the procedure, thirty <br/ ><br>minutes after the procedure, one week, three weeks, and three months.
- Secondary Outcome Measures
Name Time Method To Compare the two techniques with regards to- <br/ ><br>a)Shoulder pain and disability index (SPADI) <br/ ><br>b) Range of motion (ROM) <br/ ><br>c) Complications if any <br/ ><br>Timepoint: SPADI will be recorded before the procedure, and one week, three weeks, and 3 <br/ ><br>months after the block.