Rotator cuff tendinopathy. Unsp rotatr-cuff tear/ruptr of left shoulder, not trauma.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Tendinopathy of Rotator Cuff ?Adults (16-70 years) At least 6 weeks from the onset of pain
Exclusion criteria
Exclusion criteria: Pregnant or lactating Women Active systemic rheumatologic disorders Coagulopathies or on anticoagulant medication Diabetes mellitus Active septic disorders or history of cancers or tumors around the site of shoulder joint Use of systemic corticosteroid drugs recently in one month
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity based on visual analogue scale. Timepoint: Measuring the severity of pain at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: Visual Analogue Scale (VAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Range of Motion (ROM). Timepoint: Measuring the range of motion at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: Goniometer.;Adverse events (e.g., Inflammation in the injection site). Timepoint: Inflammation in the injection site at the first week of study after the injection. Method of measurement: Hyperemia, warmth, pain, tendonitis, tenderness.;The disabilities of the arm, shoulder and hand. Timepoint: Measuring the disabilities of the arm, shoulder and hand at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: The Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire.;Quality of life. Timepoint: Measuring the Quality of life at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: QOL-BREF Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahid Beheshti University of Medical Sciences