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Comparison of therapeutic effect of prolotherapy by glucose, corticosteroid and physical therapy in shoulder teddinopathy

Phase 3
Conditions
Injury or partial tearing of rotator cuff tendons of the shoulder.
Unspecified disorder of synovium and tendon
Registration Number
IRCT20101113005172N4
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
114
Inclusion Criteria

Shoulder pain for at least 6 weeks
Rotator cuff tendinopathy has been confirmed by physical examination and imaging methods
Patient between 18-65 years old

Exclusion Criteria

Past history of shoulder surgery
Diabete mellitus
Malignancy
Immune insufficiency disorders

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain scale and disability in patients with injury or partial tearing of rotator cuff tendons of the shoulder. Timepoint: Measure the pain and disability of the shoulder joint at the beginning of the study (before the intervention) and one week, one month and three months after the end of the treatment interventions. Method of measurement: Numerical Rating Scale and Shoulder Pain And Disability Index.
Secondary Outcome Measures
NameTimeMethod
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