To compare the effectiveness of shoulder joint dilatation with suprascapular nerve block as a treatment of frozen shoulder
- Conditions
- Health Condition 1: M750- Adhesive capsulitis of shoulder
- Registration Number
- CTRI/2020/06/025885
- Lead Sponsor
- ot Applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 73
a) Age 40ââ?¬â??70 years (M & F)
b) Spontaneous onset of Pain full & stiff joint for 4 weeks i. e presenting at the Frozen stage of Adhesive capsulitis
c) Shoulder pain that interferes with activities of daily living / work
d) Night pain mostly on lying on the involved shoulder.
e) Pain full restriction of both Active & Passive shoulder ROM (Abduction & External rotation > 50% restriction)
f) Normal radiological appearance on x-ray
g) No obvious crepitus on movement.
a) History of significant trauma to the shoulder
b) Tear of rotator cuff on clinical examination
c) Pathologic findings / Glenohumeral osteoarthritis on Radiographic evaluation
d) Clinical evidence of significant cervical spine disorder
e) Inflammatory joint diseases affecting the shoulder
f) CVA affecting the shoulder
g) Local corticosteroid injection to shoulder joint within the last 3 weeks
h) Any surgical intervention , dislocations, fractures in the affected shoulder
i) Any coronary / post coronary artery bypass catheterization before the clinical appearance of frozen shoulder
j) Any disease or medication that might have worsened physical function and interfered with the evaluation of shoulder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the effect of ultrasound guided supra scapular nerve block & hydro dilatation & physiotherapy in providing pain relief and improving the range of motion & function of shoulder jointTimepoint: To assess the effects at pre treatment , after 1st & 6 weeks post treatment
- Secondary Outcome Measures
Name Time Method Improvement of quality of life on the basis of range of motion & SPADI scale improvementTimepoint: Improvement of quality of life assessed at 1st & 6 weeks of post treatment