Comparison of the effectiveness of PRP, ozone and corticosteroids in reducing pain in patients with post-anthesis bursitis. Soft tissue disorders related to use, overuse and pressure
Conditions
Interventions
Intervention 1: Intervention group1: Patients in the LCI group: 40 mg of prednisolone and one milliliter of 1% lidocaine are injected under ultrasound guidance. Intervention 2: Intervention group2: Pa
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Diagnosis of post-anthesis bursitis based on clinical features and imaging by a specialist physician Duration of infection at least 3 months
Exclusion criteria
Exclusion criteria: Having other knee diseases at the same time, such as advanced osteoarthritis Having systemic diseases such as rheumatoid arthritis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of pain. Timepoint: Determination and comparison of the amount and severity of pain is measured at regular intervals such as before treatment, 1 month, 3 months, and 6 months after treatment. Method of measurement: Using standard pain scales such as the Visual Analogue Scale (VAS) and Numerical Rating Scale (NRS), the patient rates the intensity of their pain from 0 (no pain) to 10 (the most severe pain possible). | — |
Secondary
| Measure | Time frame |
|---|---|
| Improve performance. Timepoint: Similar to the main outcome variable (before treatment, 1 month, 3 months and 6 months after treatment). Method of measurement: Using performance assessment questionnaires such as the WOMAC Knee Performance Questionnaire and the Activities of Daily Living (ADL) Questionnaire, which assesses the patient's ability to perform daily activities such as walking, climbing stairs, etc. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarhad Saleh Nia
Hamedan University of Medical Sciences
Outcome results
None listed