High-intensity laser versus standard physical therapy for knee osteoarthritis
Official title: Rehabilitation of Knee Osteoarthritis by High Intensity Laser Therapy vs Classical Modalities
Run by Erbil Polytechnic University · NCT07551245 · Data updated 2026-11-12
This trial will try high-intensity laser therapy plus exercises against standard physical therapy plus exercises in adults aged 40–75 with mild-to-moderate knee osteoarthritis to see which reduces pain and improves knee function.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 30 Years to 60 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Erbil Polytechnic University Academic / other |
| Locations | 1 site (Erbil, Erbil Governorate) |
| Status | Recruiting |
| Started | April 20, 2026 |
| Main results expected | January 15, 2027 |
| Study ends | January 20, 2027 |
| Registry record updated | April 24, 2026 |
| Trial ID | NCT07551245 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 40–75 years old with clinical and radiographic knee osteoarthritis (Kellgren-Lawrence grades 1–3) who can attend treatment sessions and provide informed consent are ideal candidates.
✕Probably not a fit
People with severe (Kellgren-Lawrence grade 4) knee OA, recent knee surgery, active infection, photosensitivity, epilepsy, active malignancy, or other contraindications to laser therapy are unlikely to benefit or be eligible.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a randomized comparative trial enrolling 100 adults with ACR-confirmed knee osteoarthritis at rehabilitation centers in Erbil, Iraq. Participants will be randomly assigned to receive either high-intensity laser therapy combined with therapeutic exercise or conventional physical therapy modalities combined with the same exercise program. The primary outcome is pain intensity at four weeks measured by WOMAC/VAS, with additional assessments of joint function, MRI structural changes, and laboratory markers of inflammation and cartilage health over follow-up. Safety and adverse events related to the interventions will also be recorded.
Why it matters
Potential benefit: If successful, high-intensity laser therapy could provide faster pain relief and better knee function than conventional modalities, potentially reducing disability and reliance on medications.
How similar studies have gone: Low-level laser therapy has produced mixed results in knee OA and high-intensity laser therapy is less studied but has shown promising results in small, limited trials.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of Knee Osteoarthritis: Patients must have a clinical and radiographic diagnosis of knee OA according to the American College of Rheumatology (ACR) criteria, including evidence of joint space narrowing, osteophyte formation, and other degenerative changes observed on X-rays or MRI. Age: Adults aged between 40 and 75 years. Willingness to Participate: Participants must provide informed consent and be willing to adhere to the study protocol, including attending all treatment sessions and follow-up assessments. Kellgren-Lawrence Grade: Patients with knee OA grades 1-3 (mild to moderate OA). Exclusion Criteria: * Contraindications to Laser Therapy: Active malignancy History of epilepsy Photosensitivity disorders Active infection in the treatment area Surgical History: Patients who have undergone knee surgery within the past 6 months Scheduled surgery during the study period Advanced Disease: Kellgren-Lawrence Grade 4 (severe OA) where surgical intervention is indicated Pregnancy or Lactation: Pregnant or lactating women Severe Comorbidities: Uncontrolled diabetes Severe cardiovascular disease Neurological disorders that might interfere with participation or affect treatment outcomes
Where it's running
-
Aylan Center
Erbil, Erbil Governorate, Iraq Recruiting
Study contacts
- Study coordinator: Mahdi Qadir, PhD
- Email: mahdiqader@epu.edu.iq
- Phone: +9647504631542
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.