PRP in tendonitis

Phase 3

Recruiting

• Conditions: shoulder tendonitis.; Rotator cuff tear or rupture, not specified as traumatic; M75.1

• Registration Number: IRCT20220803055610N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Pain is the most common symptom.
Physical examination findings include pain on movement, weakness and positive tests
Diagnosis of rotator cuff tendinopathy with musculoskeletal ultrasound
Symptoms have been persistent for more than 3 months and conservative treatment has failed for at least 4 weeks of formal medical treatment and physical therapy.

Exclusion Criteria

Full-thickness rotator cuff tear
Current treatment with anticoagulation
Steroid injection in the past 6 months in the injuredshoulder
Prior PRP treatment to the injured shoulder
Bleeding disorders or preoperative platelet countless than 50,000
Presence of another disease that may causeshoulder pain and dysfunction as rheumatoidarthritis
Prior surgery to the injured shoulder

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Every 2 weeks to eight weeks. Method of measurement: VAS score.;Range of motion. Timepoint: Every two weeks to three months. Method of measurement: Goniometer.;Ultrasound Findings. Timepoint: At the beginning of the study and after 3 months. Method of measurement: Ultrasound probe.