Pregabalin Phonophoresis and MET for Knee Osteoarthritis

Inclusion Criteria: 1. Diagnosed Grade III knee osteoarthritis confirmed by Kellgren-Lawrence grading scale (radiograph within past 12 months or newly obtained). 2. Neuropathic pain component confirmed by DN-4 questionnaire (score ≥4). 3. Age between 40 and 70 years inclusive. 4. Both male and female participants. 5. Unilateral or bilateral knee involvement (if bilateral, the more symptomatic knee selected for assessment and treatment). 6. Willing and able to provide written informed consent. 7. Available to attend 4 sessions per week for 4 consecutive weeks (total 16 sessions). 8. Able to understand and follow verbal instructions (for MET). Exclusion Criteria: 1. Diabetic neuropathy (diagnosed or DN-4 score attributable to diabetes rather than knee OA). 2. Active skin lesions, wounds, infections, or dermatitis on the knee or calf. 3. Metal implants (including knee replacement), pacemaker, or other electronic implant (contraindications for ultrasound). 4. Received intra-articular knee injection (corticosteroid or hyaluronic acid) within the last 3 months. 5. Grade I, II, or IV knee osteoarthritis (Kellgren-Lawrence). 6. Aseptic arthritis of knee (rheumatoid, psoriatic, gouty). 7. Any lower extremity deformity (genu varum \>15°, genu valgum \>15°, fixed flexion deformity \>15°). 8. Previous knee replacement surgery (partial or total). 9. Known allergy or hypersensitivity to pregabalin, gabapentin, or any gel components. 10. Pregnant or lactating women (ultrasound safety in pregnancy not established for non-obstetric use). 11. Concurrent participation in another interventional study. 12. Diagnosis of fibromyalgia, complex regional pain syndrome, or other centralized pain disorder that might confound neuropathic pain assessment. 13. Active malignancy or history of knee malignancy. 14. Deep vein thrombosis or thrombophlebitis in lower limb.