Tendonitis. Unspecified rotator cuff tear or rupture, not specified as traumatic
Conditions
Interventions
Intervention 1: First intervention group: Patients receive PRP injections, administered twice with a one-month interval. Changes are measured during this period and one month after the final injection
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: Shoulder pain for more than 3 months Age over 40 years old Complete rupture of the rotator cuff tendons Fibromyalgia and polymyalgia rheumatica Thrombocytopenia (platelets less than 150,000) 2) Increase in platelet count to 2 to 3 times the baseline after centrifugation
Exclusion criteria
Exclusion criteria: Presence of radicular pain Presence of inflammatory disorders such as rheumatoid arthritis Presence of other pathologies that can lead to shoulder pain, such as frozen shoulder Having loose ligaments Having a shoulder dislocation Having had a cortisone injection in the shoulder joint within the past 3 months Use of physiotherapy modality in the last 3 months Use of nonsteroidal anti-inflammatory drugs during the week before the injection Having anemia (hemoglobin less than 11) Pregnancy (nonsteroidal anti-inflammatory drugs)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Every 2 weeks to eight weeks. Method of measurement: Visual Analog Scale (VAS degree).;Range of motion. Timepoint: Every two weeks to three months. Method of measurement: Gunya meter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyed Khalil Pestehei?Dr. Ramin Kordi
Tehran University of Medical Sciences
Outcome results
None listed