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Clinical Trials/IRCT20220803055610N1
IRCT20220803055610N1RecruitingPhase 3

Evaluation of the effect of platelet-rich plasma in the treatment of shoulder tendonitis

Tehran University of Medical Sciences0 sites200 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
Phase 3
Status
Recruiting
Enrollment
200
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
30 years to 60 years (—)
Sex
All

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

Investigators

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PRP in tendonitis | Clinical Trial