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Effect of ultrasound guided intra-articular injection of corticosteroids and platelet-riched plasma in the treatment of rotator cuff tendinopathy

Phase 3
Recruiting
Conditions
Rotator cuff tendinopathy.
Rotator cuff tear or rupture, not specified as traumatic
M75.1
Registration Number
IRCT20221029056333N3
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Shoulder pain that lasts more than three months
Tendinopathy and partial rupture of rotator cuff tendons
MRI findings of tendinopathy or incomplete rotator cuff tear

Exclusion Criteria

Complete rupture of rotator cuff tendons
History of shoulder surgery in the last 6 months
Presence of rheumatological inflammatory diseases
Shoulder instability is based on examinations
The history of corticosteroid injection in the shoulder joint in the last 3 months
History of PRP treatment in the last 6 months
Dissatisfaction of patients

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before treatment and 1, 2, 3, and 6 months after the start of treatment. Method of measurement: Using the VAS scale & record severe pain intensity.;Shoulder range of motion. Timepoint: Before treatment and 1, 2, 3, and 6 months after the start of treatment. Method of measurement: By goniometer.
Secondary Outcome Measures
NameTimeMethod
Patients' performance. Timepoint: Before treatment and 1, 2, 3, and 6 months after the start of treatment. Method of measurement: Disabilities of the Arm, Shoulder and Hand Outcome ?? DASH.
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