patients with painful and restricted shoulder shoulder pain, dextrose, nerve pain, range of motion, neurodynamic techniques, prediction factor
Conditions
Interventions
Experimental group will receive conventional treatments plus a three-week course of 5% dextrose injection.
Conventional treatments include medication, physical therapy, and rotator cuff interval injec
Experimental Other,Active Comparator Other
5% dextrose injection group,Comparison group
Sponsors
Individual
Eligibility
Sex/Gender
All
Age
20 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. The intensity of shoulder pain on either side is more than 2 points on a numeric rating scale. 2. Shoulder mobility restriction in any direction
Exclusion criteria
Exclusion criteria: 1. Any structural problems on shoulder joint, e.g. rotator cuff tear and glenohumeral arthritis. 2. History of shoulder fracture or surgery. 3. Systemic neuromuscular disease. 4. Pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shoulder mobility (range of motion) Baseline, 1st, 2nd, 3rd, 6th, 12th week Goniometer | — |
Secondary
| Measure | Time frame |
|---|---|
| Nerve mechano-sensitivity Baseline, 1st, 2nd, 3rd, 6th, 12th week Neurodynamics test ,Function Baseline, 1st, 2nd, 3rd, 6th, 12th week PENN Shoulder Score, Patient Specific Functional Scale, ,Overall improvement 2nd, 3rd, 6th, 12th week Global Rating of Change Scale ,Pain intensity Baseline, 1st, 2nd, 3rd, 6th, 12th week Numeric rating scale | — |
Countries
Taiwan
Contacts
Public ContactPing Chun Yeh
Fu Jen Catholic University Hospital
Outcome results
None listed