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Can regenerative photonic therapy improve pain and mobility in knee osteoarthritis?

Efficacy of regenerative photonic therapy (RPT) plus exercises versus exercises for the treatment of knee osteoarthritis in geriatric care: a randomized placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN34726586
Enrollment
60
Registered
2013-11-08
Start date
2012-10-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee osteoarthritis Musculoskeletal Diseases Gonarthrosis [arthrosis of knee]

Interventions

The treatment group will receive regenerative photonic therapy (RPT) plus exercises while the control group will receive placebo (dummy) RPT and exercises.

Sponsors

International Medical Instruments Inc. (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 50-85 years old 2. Patients suffering from chronic (more than 6 months duration) knee osteoarthritis (OA) pain 3. Able to provide informed consent in a written form

Exclusion criteria

Exclusion criteria: 1. Surgical joint replacement 2. Radiological grade 1 and 4 osteoarthritis 3. Oral opioid or steroid medications 4. Recent ( 11, or glucose in urine) 17. Neurological manifestations (numbness, paraesthesia, loss of sensitivity anywhere in the body) 18. Known autoimmune diseases (e.g., lupus, rheumatoid arthritis)

Design outcomes

Primary

MeasureTime frame
1. Western Ontario and McMaster Universities Arthritis Index (WOMAC) subscale difficulties performing daily activities (DPDA) 2. Walking pain by Visual Analog Scale (VAS, 0 = no pain, 10 = worst possible pain) Primary outcomes will be measured upon completion of 6 weeks treatment, at one month and six months follow-up.

Secondary

MeasureTime frame
1. WOMAC Total 2. WOMAC Pain subscale 3. The highest weekly pain by Visual Analog Scale (VAS, 0 = no pain, 10 = worst possible pain) 4. Pain medication intake (amount of pain pills per day) Secondary outcomes will be measured upon completion of 6 weeks treatment, at one month and six months follow-up.

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026