Sacroiliac joint pain. Chronic pain, not elsewhere classified
Conditions
Interventions
Intervention group: PRP injection (Royagen kits, made by Aria Mobna Diagnos Company) is performed as a single dose with a volume of 10 cc..
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients aged 20-60 years with sacroiliac joint pain and an NRS (Numeric Rating Scale) score greater than 5 during the last three months, based on clinical examinations and positive results of three sacroiliac joint provocative tests (Faber, Gaenslen, iliac compression, Fortin Finger, Yeoman, thigh thrust, iliac distraction), will be included in the study.
Exclusion criteria
Exclusion criteria: Thrombocytopenia (platelets less than 150,000 per microliter), local infection at the injection site, use of non-steroidal anti-inflammatory drugs within 48 hours before injection, use of systemic corticosteroids within a month before injection, malignancy, pregnancy, rheumatological diseases, Uncontrolled hormonal disorders, systemic inflammatory diseases, neurological or psychological disorders, age less than 20 years or more than 60 years, patients with midline pain above the level of the fifth lumbar vertebra.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Intensity. Timepoint: The patient's pain intensity is measured before the intervention and at one and three months after the intervention (PRP injection into the sacroiliac joint). Method of measurement: Numeric Rating Scale (NRS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Functionality. Timepoint: The patient's functional improvement is measured before the intervention and at one and three months after the intervention (PRP injection into the sacroiliac joint). Method of measurement: Oswestry Disability Index (ODI). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Hossein Majedi Ardakani
Tehran University of Medical Sciences
Outcome results
None listed