Shoulder Adhesive Capsulitis Adhesive Capsulitis Capsulitis, Adhesive Frozen Shoulder Shoulder, Frozen Adhesive Capsulitis of the Shoulder Shoulder Adhesive Capsulitis
Conditions
Interventions
PRP therapy: A single dosage of 4 mL of PRP mixed with 1 mL of 2% lidocaine in a 22-gauge spinal needle under aseptic conditions will be inserted in the affected joint.
Proprioceptive Neuromuscular
IR (arm at side), Theraband exercise
Treatment session: 30 minutes of each session
4 times a week for up to 6 weeks.,Sham PRP therapy: A single dosage of 1 mL of 2% lidocaine in a 22-gauge spinal needle under aseptic conditions will be inserted in the affected joint.
Proprioceptiv
IR (arm at side), Theraband exercise
Treatment session: 30 minutes of each session
4 times a week for up to 6 weeks.
Experimental Other,Sham Comparator Other
Platelet Rich Plasma (PRP) with Physiotherapy ,Sham Platelet Rich Plasma (PRP) with Physiotherapy
Sponsors
Department of Physiotherapy and Rehabilitation, Jashore University of Science and Technology, Jashore 7408, Bangladesh.
Eligibility
Sex/Gender
All
Age
20 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Individuals aged 20 to 65 years 2. Who have experienced shoulder pain for less than three months, 3. Pain aggravated by shoulder movement and 4. Notable passive range of motion limitations in more than one plane.
Exclusion criteria
Exclusion criteria: 1. Bilateral adhesive capsulitis. 2. Prior glenohumeral joint injection within the last six months. 3. Previous medication use or surgical intervention for adhesive capsulitis, or manipulation under anesthesia. 4. Participants having present with neurologic impairments affecting shoulder function during activities of daily living. 5. Confirmed brachial plexopathy via nerve conduction study. 6. Pain or pathology in adjacent joints (cervical spine, elbow, wrist, or hand), or 7. Any contraindications to injection therapy such as local cellulitis, septic arthritis, or acute fracture
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pressure pain threshold Baseline and after completion of intervention Pressure pain algometer,Cell count of the RBC, WBC and T cell Baseline and after completion of intervention Microscopic examination of aspirated synovial fluid of affected shoulder joint,Soft tissue morphology (length and diameter) of supraspinatus, infraspinatus, biceps and pectoralis major muscles Baseline and after completion of intervention Musculoskeletal Ultrasound (MSK-USG) | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional activity of shoulder joint Baseline and after completion of intervention Shoulder Pain and Disability Index (SPADI) | — |
Countries
Bangladesh
Contacts
Public ContactDr. K M Amran Hossain
Lecturer, Department of Physiotherapy and Rehabilitation
Outcome results
None listed