Condition 1: Rotator cuff tendinopathy. Condition 2: Rotator cuff tendinopathy. Rotator cuff tear or rupture, not specified as traumatic Rotator cuff tear or rupture, not specified as traumatic
Conditions
Interventions
Intervention 1: Intervent group:100 units botulinum toxin dysport single dose subacromialion. Intervention 2: Control group: 40 mg of methylprednisolone with lidocaine single dose subacromial.
Sponsors
Artesh University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients who have no history of shoulder surgery, patients who are fully followed up during the intervention, and those who consent to participate in the study. Patients who have received other treatments and have not received an adequate response.
Exclusion criteria
Exclusion criteria: Patients who have a history of shoulder surgery, patients who are not fully followed up during the intervention, those who do not consent to participate in the study, active infection, breastfeeding, pregnancy, myasthenia gravis, aminoglycoside use, allergy to Botulinum toxin or corticosteroid.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of pain. Timepoint: At the beginning of the study, one and three months after the intervention. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: Before the intervention, one and three months later. Method of measurement: SF36 questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElaheh Asadi amin abadi
Artesh University of Medical Sciences
Outcome results
None listed