Adhesive capsulitis of shoulder. Adhesive capsulitis of shoulder
Conditions
Interventions
Intervention 1: Intervention group: 8 ml of PRP is injected once. To prepare PRP, 15 ml of the patients blood will be drawn. PRP is prepared using a double-spin centrifugation technique. Blood will be
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Unilateral shoulder pain and limitation of active and passive movements in at least two directions of the glenohumeral joint (abduction, flexion, external rotation, and internal rotation) for more than one month (but less than one year) Age above 18 years Shoulder pain for at least one month with greater than one-third loss of active shoulder flexion, abduction, and external rotation Anterior-posterior normal radiograph of the glenohumeral joint in normal rotation Willingness to participate in the study and forgoing any other treatment method
Exclusion criteria
Exclusion criteria: Unwillingness to participate in the study History of previous shoulder trauma/surgery Patients with local infection in the shoulder, systemic infection or inflammatory disease (such as rheumatoid arthritis and hepatitis) Patients with chronic diseases (chronic kidney failure, chronic liver disease) Patients with a history of diabetes or malignancy (hematological or non-hematological) Pregnancy or breastfeeding Patients with blood disorders or under antiplatelet or anticoagulant treatment Drug sensitivity to steroids Taking antitumor or immunosuppressive drugs Corticosteroid injection to the shoulder in the previous 6 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shoulder pain and disability index score. Timepoint: Before intervention and 3, 6, 12, 24 weeks after the intervention. Method of measurement: Shoulder pain and disability index tool.;The visual analog scale for pain score. Timepoint: Before intervention and 3, 6, 12, 24 weeks after the intervention. Method of measurement: The visual analog scale for pain.;Quick disabilities of the arm, shoulder, and hand questionnaire score. Timepoint: Before intervention and 3, 6, 12, 24 weeks after the intervention. Method of measurement: Quick disabilities of the arm, shoulder, and hand questionnaire.;Joints' range of motion. Timepoint: Before intervention and 3, 6, 12, 24 weeks after the intervention. Method of measurement: Universal goniometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Hosein Ebrahimzadeh
Mashhad University of Medical Sciences
Outcome results
None listed