Health Condition 1: M170- Bilateral primary osteoarthritis of knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: **Inclusion Criteria:** 1. Male and female adults aged 18 years or older 2. Radiological diagnosis of multicompartmental knee osteoarthritis 3. Joint pain of 60 mm or more according to the Visual Analog Scale (range 0–100 mm) 4. Radiological severity classified as Grade I to III on the Kellgren–Lawrence scale 5. Body Mass Index (BMI) less than 30 kg/m² 6. Availability for examination during the follow-up period
Exclusion criteria
Exclusion criteria: Body Mass Index more or equal to 30 Diagnosis of polyarticular disease • Severe mechanical deformity (bidiaphyseal varus, 4; valgus, 16) • Previous Knee surgery • Hyaluronic acid or corticosteroid injections within the last 3 months. • Diagnosis of systemic autoimmune rheumatoid disease (connective tissue disease and systemic necrotizing vasculitis) • Uncontrolled diabetes mellitus (glycosylated hemoglobin more than 7 percent ) • Blood disorders (thrombopathy, thrombocytopenia, anemia with hemoglobin level less than 9) • Ongoing immunosuppressive and or dicumarinic therapy • Use of non-steroidal anti-inflammatory drugs within 15 days before inclusion in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To Evaluate functional outcomes of Plasma Rich in Growth Factors (PRGF) and Platelet-Rich Plasma (PRP) in osteoarthritis of Knee.Timepoint: baseline day 14, 1 month, 3 months, 6 months, and 12 months post injection. | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effects of Plasma Rich in Growth Factors (PRGF) & Platelet-Rich Plasma (PRP) on pain, cartilage repair, patient satisfaction & safety.Timepoint: baseline day 14, 1 month, 3 months, 6 months, & 12 months post injection. | — |
Countries
India
Contacts
KLE University of Higher Sciences and Research