Role of ultrasound guided shoulder joint hydrodistension in the management of frozen shoulder
- Conditions
- Health Condition 1: M678- Other specified disorders of synovium and tendon
- Registration Number
- CTRI/2023/12/060642
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Adult patients having clinically diagnosed shoulder joint Adhesive capsulitis with persistent pain and functional deficit for more than three months not resolving with conservative management.
1. Patients with other causes of shoulder pain like osteoarthritis, inflammatory joint disease, rotator cuff tear and secondary adhesive capsulitis (shoulder injury or surgery).
2. Patients with underlying coagulopathies or taking anti-coagulant medications
3. Patients with local site infection
4. Patients who have received prior corticosteroid injection or have undergone arthroscopic or open capsular release surgery
5. Shoulder joint plain radiographic finding of significant glenohumeral joint arthritis
- History of side effects to local anaesthetics, corticosteroids.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To study the improvement in range of movement (ROM) after ultrasound guided hydrodistension of glenohumeral joint. <br/ ><br>2. To assess the improvement in shoulder pain status after hydrodistension <br/ ><br>3. To assess the functional improvement after hydrodistension. <br/ ><br>4. To compare the pain, range of movement & functional improvement between study & control groupTimepoint: At 4 weeks & 12 weeks
- Secondary Outcome Measures
Name Time Method To record the complications if any associated with the procedure.Timepoint: At 4 weeks & 12 weeks