Investigating the Effect of Platelet-Rich Plasma in Arthroscopy
Phase 2
Recruiting
- Conditions
- Small and medium rotator cuff tears of the shoulder.Small and medium rotator cuff tears of the shoulderM65-M68
- Registration Number
- IRCT20220803055610N2
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
age between 18 and 70 years old
symptoms of rotator cuff tears
MRI findings of minor to medium rotator cuff tears
Exclusion Criteria
a history of shoulder surgery, achronic dislocation or pyogenic infection, or rotator cuffarthropathy with glenohumeral osteoarthritis
a large ormassive tear (anteroposterior size > 30 mm) during surgery
pregnant or lactating women
rheumatoid arthritis
gout
blood diseases
severe cardiovascular dis-eases
infections
immunodepression
patients receiving anticoagulant therapy
patients with haemoglobin values < 11 g/dl and platelet values < 150, 000/mm 3.
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.
- Secondary Outcome Measures
Name Time Method