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Efficacy of a Home-Use Photobiomodulation Device for the Treatment of Patients With Knee Osteoarthritis

Evaluation of the Efficacy of a Home-Use Photobiomodulation Device for the Treatment of Patients With Knee Osteoarthritis: An Open Label, Single-Arm Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05357703
Acronym
PBM&KOA-02
Enrollment
30
Registered
2022-05-03
Start date
2022-05-26
Completion date
2023-08-15
Last updated
2022-06-01

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

Conditions

Knee Osteoarthritis

Keywords

Photobiomodulation, Low-Level Laser Therapy

Brief summary

Osteoarthritis is a degenerative disease affecting joint cartilage and its surrounding tissue. It is the leading cause of disability in the elderly. Photobiomodulation (PBM), has been used widely for alleviation of pain, reduction of inflammation, and acceleration of wound healing, and particularly to treat knee osteoarthritis (KOA). The purpose of the current study is to determine if B-Cure laser treatments, applied at home, by the patient or personal caregiver in a real-life situation, can reduce pain and improve functionality in patients with KOA.

Detailed description

Eligible patients with knee osteoarthritis will receive a B-Cure laser device for self-application at home in addition to standard care. Patients will be invited to the clinic for 3 visits: baseline, 1, and 2 months. Evaluations at the visits will include physical examination, knee range of motion, time up&go test, and patient reported outcomes including subjective pain level by visual analogue scale (VAS), functional and quality of life questionnaires. The study hypothesis is that B-Cure laser treatments, applied, at home, by the patient, can ameliorate KOA related inflammation thereby reducing pain and improving functionality in these patients.

Interventions

DEVICEStandard treatment + Active B-Cure laser

The B-Cure laser pro is a portal, non-invasive, photobiomodulation device, that emits light in the near infrared (808nm) over an area of 1X4.5 cm2 with power output of 250mW, and energy dose of 5J/minute.

Sponsors

Holy Family Hospital, Nazareth, Israel
CollaboratorOTHER
Erika Carmel ltd
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnoses of knee osteoarthritis by American College of Rheumatology (ACR) 2. Kellgren & Lawrence classification 2-3 3. Knee pain on movement 40 to 90 mm Visual Analog Scale 4. Knee pain and related functional reduction for the last ≥ 3 months 5. Agrees not to use NSAIDs throughout the experiment

Exclusion criteria

1. Pregnant or nursing, or with the ability to become pregnant and not using an accepted form of birth control 2. Other causes of knee-related pain (e.g. hip OA, arterial insufficiency, radiculopathy etc) have been ruled out by physical examinations. 3. Knee surgery for KOA 4. Intra-articular steroid injection and/or oral steroid treatment within the last six months 5. Rheumatoid arthritis 6. Active malignancy 7. Uncontrolled diabetes mellitus 8. Neurological conditions: sciatica, neuropathy, multiple sclerosis 9. Other chronic pain conditions that may affect results: Fibromyalgia, back pain, hip pain 10. Has any photobiomodulation (low level laser) device at home or has previously used photobiomodulation for knee pain 11. Has known dermatological sensitivity to light 12. Enrolled in any other clinical trial within the last 6 weeks or enrollment in another clinical trial during participation in this trial. \-

Design outcomes

Primary

MeasureTime frameDescription
level of painone monthChange from baseline in pain score by VAS

Secondary

MeasureTime frameDescription
Change from baseline in WOMAC score [ time point - 1 month]one monthThe WOMAC is a disease-specific tool used for people with hip or knee OA to measure physical function, pain, and stiffness. It widely used in clinical studies as primary or secondary outcome.

Countries

Israel

Contacts

Primary ContactJehad Khazen, MD
khazenjehad@gmail.com+972545600095

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026