Health Condition 1: M750- Adhesive capsulitis of shoulder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Clinically diagnosed case of frozen shoulder (ICD 11-FB53.0)suffering from at least 3 months. 2. Age between 18 and 65 years. 3. Participants of either sex or transgender. 4. Patients who are currently receiving NSAID therapy or regular oral or topical analgesics for painful episodes of frozen shoulder, as long as the drugs are stopped entirely at least two weeks before trial participation.
Exclusion criteria
Exclusion criteria: 1. Severe restriction of shoulder range of motion (ROM) Elevation (vertical arm raise) or abduction: 0? to 30? External or internal rotation in abduction: 0? to 30? 2. Cases willing for or requiring immediate surgical intervention or undergoing major shoulder surgery in last 6 month. 3. Not provided with written informed consent of participation. 4. Patients with known primary muscle disorders (e.g., inflammatory myopathies, muscular dystrophies, or other clinically significant myopathic conditions) affecting shoulder function. 5. Participants with clinical suspicion or ultrasonographic evidence of secondary shoulder pathology (rotator cuff tear, bursitis, arthritis, calcific tendinitis, etc.) 6. Non-ambulatory patients. 7. Intra-articular injections within 2 weeks before study entry. 8. Patients who are too sick for consultation. 9. Diagnosed cases of uncontrolled systemic diseases, unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life. 10. Pregnancy, puerperal women and lactating mother. 11. Tobacco chewing and/or smoking, alcoholism and/or any form(s) of substance abuse and/or dependence (TAPS tool) 12. Self-reported immune-compromised state, AIDS, hepatitis etc. 13. Undergoing homoeopathic treatment for any chronic disease within last 6 months. 14. Simultaneous participation in any other clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shoulder Pain And Disability Index (SPADI)Timepoint: At baseline, monthly, up to 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Penn shoulder score (PSS)Timepoint: At baseline, monthly, up to 3 months;Measure Yourself Medical Outcome profile version 2 (MYMOP-2)Timepoint: At baseline, monthly, up to 3 months;Goniometric measurements of restricted range of motion of shoulderTimepoint: At baseline, and after 3 months;Time (days) to complete recoveryTimepoint: Baseline, up to 3 months | — |
Countries
India
Contacts
D. N. De Homoeopathic Medical College and Hospital