CTRI/2017/08/009550
Completed
Phase 4
A comparative study on efficacy of suprascapular nerve block versus subacromial steroid injection in shoulder impingement syndrome.
IPGMER SSKM Hospital0 sites70 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- IPGMER SSKM Hospital
- Enrollment
- 70
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Clinically suggestive and USG and/or MRI confirming Neer Stage I \& II impingement.
- •(2\) Not sufficiently responding to conservative treatment over 8weeks.
- •(3\) Aged 20 to 60 years.
- •(4\) Pain defined as a score of 5 points or more on a 10\-cm visual analog scale (VAS) rated from 0 (no pain) to 10 (worst imaginable pain).
- •(5\) Patient mentally sound enough to communicate and participate in the study and can understand the parameters well.
Exclusion Criteria
- •1\. USG showing Rotator cuff tear.
- •2\. Bleeding or clotting disorders.
- •3\. Patients refusing intervention or participation.
- •4\. The presence of another obvious associated cause for the pain (i.e., Primary osteoarthritis of glenohumeral joint, fracture, radiculopathy, myofascial pain, central neuropathic pain)
- •5\. Severe motor weakness (muscle power of deltoid less than grade 2 on the manual muscle test).
- •6\. Patients with Post myocardial infarction, Post stroke, Post mastectomy, prolonged immobilization.
- •7\. The presence of an unstable medical condition or a known uncontrolled systemic disease, including cancer, diabetes, rheumatoid arthritis, endocrine disease,
- •major depression, schizophrenia, \& patients with persistent very high level of ESR \& CRP.
- •8\. Patients with contraindications of steroid injections i.e. overlying soft tissue sepsis, bacteraemia, anatomic inaccessibility, uncooperative patient, uncontrolled bleeding diathesis etc.
- •9\. Patients who got intra\-articular injection in shoulder within last six months.
Outcomes
Primary Outcomes
Not specified
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