About this trial
This clinical trial will evaluate the effects of High-Intensity Laser Therapy (HILT) on femoral cartilage thickness and other clinical outcomes in people with knee osteoarthritis. Participants aged 40 to 60 years with grade II or III knee osteoarthritis will be randomly assigned to receive either HILT plus conventional physiotherapy or conventional physiotherapy alone. Both groups will receive 12 treatment sessions on alternate days for 4 weeks. The study will assess changes in cartilage thickness using ultrasound, as well as improvements in pain, knee movement, muscle strength, and daily function. Findings from this research may help improve physiotherapy treatment strategies for patients with knee osteoarthritis.
Eligibility criteria
Qualifiers
Male and female participants aged 40-60 years.
Diagnosed with knee osteoarthritis (Kellgren-Lawrence grade II or III).
Knee pain for at least 3 months.
Visual Analogue Scale (VAS) score ≥ 3.
Disqualifiers
History of knee surgery or traumatic knee injury.
Inflammatory arthritis (e.g., gout, psoriatic arthritis).
History of cancer or psychiatric illness.
Cognitive disorders (e.g., Parkinson's disease, Alzheimer's disease).
Trial design
Treatments tested in this trial
- High-Intensity Laser Therapy (HILT) + Conventional Physiotherapy
- Conventional Physiotherapy