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Effect of PRP and methylprednisolone injection in patients with partial rotator cuff tear

Phase 2
Conditions
Partial rotator cuff tear.
Injury of muscle(s) and tendon(s) of the rotator cuff of shoulder
S46.0
Registration Number
IRCT20230608058415N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
100
Inclusion Criteria

Patients with partial thickness rotator cuff tear and reduced shoulder range of motion
Patient does not have any contraindication for shoulder injection
Age more than 30

Exclusion Criteria

Patients with previous shoulder surgery and injection
Patients with frozen shoulder
Patients with shoulder fracture
Other pathologies induce shoulder pain (in examination and radiology)
Patients with full thickness rotator cuff tear

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Shoulder function. Timepoint: Before injection, 3 & 6 months after injection. Method of measurement: Constant-Merely.
Secondary Outcome Measures
NameTimeMethod
Shoulder pain. Timepoint: Before injection, 3 & 6 months after injection. Method of measurement: Visual Analogue Scale.
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