Health Condition 1: null- Patients with Chronic shoulder pain of 3 months duration with NRS 5 not responding to conservative therapies will be included in the study Health Condition 2: M659- Synovitis and tenosynovitis, unspecified
Conditions
Interventions
Intervention1: group LS: SSN block will be given with bupivacaine (0.5%) and methylpredinisolone (40 mg) total of 5 ml under ultrasound guidance over 1-2 minutes
Control Intervention1: GROUP PRF: SSN
Sponsors
PGIMER Chandigarh
Eligibility
Inclusion criteria
Inclusion criteria: Chronic shoulder pain of >3 months duration with NRS > 5 diagnosed with any of the mentioned conditions like chronic tendinitis, impingement syndrome, frozen shoulder secondary to arthritis, chronic rotator cuff injuries will be included in the study.
Exclusion criteria
Exclusion criteria: Those patients who have underlying shoulder pathology like rheumatoid arthritis or malignant disease of shoulder, who have already diagnosed with cervical herniated disc disorder pathology, prior RF treatments in last 3 months, fibromyalgia, coagulation disturbances, uncontrolled diabetes, allergies to local anesthetics, malignancy, mental disorders or psychiatric conditions preventing adequate communication and pregnancy will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of patient having significant pain relief equal to or more than 50%Timepoint: 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement in partial range of motion (PROM) at various follow up times. Shoulder Pain and Disability Index (SPADI) at various follow up times. Pain score at various follow up times. Timepoint: baseline, 2 weeks, 4 weeks, 2 month, 3 month | — |
Countries
India
Contacts
Public ContactBabita Ghai
Post Graduate Institute of Medical Education and Research
Outcome results
None listed