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Clinical Trials/IRCT20100718004409N12
IRCT20100718004409N12
Completed
Phase 3

The comparison of the effectiveness of high leukocyte PRP, low leukocyte PRP & placebo in treatment of the patients having rotator cuff tendinopathy or partial tear

Iran University of Medical Sciences0 sites75 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Condition 1: rotator cuff tendinopathy, partial tear of rotator cuff. Condition 2: Shoulder impingement.
Sponsor
Iran University of Medical Sciences
Enrollment
75
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Shoulder pain lasted more than 6 weeks
  • At least 3 positive specific shoulder tests
  • MRI findings implying tendinopathy or partial tear of rotator cuff

Exclusion Criteria

  • Shoulder pain that lasted less than six weeks
  • The presence of sensory or motor disturbances caused by the cervical radiculer pain
  • Evidence from other pathologies that can lead to shoulder pain. For example, the presence of calcified tendonitis or adhesive capsulitis and ...
  • History of shoulder surgery in the last 6 months
  • The presence of inflammatory rhomatologic diseases such as rheumatoid arthritis, fibromyalgia, poly mialia rheumatica and ...
  • Complete rupture of rotator cuff tendons based on MRI findings
  • The presence of ligamentous laxity or shoulder instability based on physical examination
  • History of corticosteroid, analgesic or hyaluronic acid injection in the shoulder joint over the past 3 months
  • History of exercise therapy and physiotherapy modalities over the past 6 weeks
  • The history of treatment with PRP in the last 6 months

Outcomes

Primary Outcomes

Not specified

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