Blue Light Device for Pain Therapy

Phase 3

Completed

Conditions: Low Back Pain
Low Back Pain, Recurrent
Musculoskeletal Pain
Chronic Pain

Interventions: Device: Pain Relief Patch
Device: Control PRP device

Registration Number: NCT01528332

Lead Sponsor: Philips Electronics Nederland BV

Brief Summary: The purpose of this study is to determine if the Pain Relief Patch, which shines light of a limited wavelength on the painful area of the back, relieves chronic musculoskeletal back pain. At the same time, this study will gather information on side effects associated with use of the Pain Relief Patch. The study will compare the Pain Relief Patch to a patch that is similar in appearance, but which shines a different, presumed nontherapeutic, wavelength of light.

Detailed Description: This study will test the Pain Relief Patch (PRP), a new device containing LEDs that is to be worn on the skin of the painful area, to see if it is effective in relieving chronic musculoskeletal back pain. It will also test the safety of the patch. The LEDs in the PRP emit a certain kind of light (peak wavelength 453 nm) that stimulates the production of nitric oxide (NO) in the skin. NO has been shown to induce a number of actions that should contribute to pain relief, including relaxation of smooth muscle cells, dilation of blood vessels, increased concentrations of oxygen in the cells and washout of metabolic byproducts and toxins caused by cell injury or death. Participants in one treatment group will be treated 5 times over 2 weeks for 30 minutes with PRP patches in the clinic. Participants in the control arm will be treated for the same length of time with a similar device that contains LEDs that emit another wavelength of light that does not induce production of NO. To prevent the influence of expectations on the results, neither the participants nor the medical staff directly responsible for their treatment will be told with which of the test patches the participants are treated. Other clinic staff will be responsible for all activities that could identify treatment arm, including putting the devices on and removing them, and examining the condition of the participants' skin before and after treatment. To get an accurate measure of how effective the devices are, participants will score their pain several times before the treatment period begins, as well as before and after each treatment. They will also complete several pain questionnaires during the study.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 171

Inclusion Criteria

Is between 18 and 65 years of age, inclusive
Is able to consent to participation by signing the informed consent form
Has had localized mild to moderate (a score ≥ 2 and ≤ 6 on a 0 - 10 point pain intensity VAS) back pain for the 3 months prior to enrollment in study or longer
Has a mean pain intensity VAS value (calculated from pain intensity VAS at Screening Visit, home assessment and pretreatment at Visit 1) between ≥ 2 and ≤6 at baseline prior to randomization
Has skin type II, III or IV on the Fitzpatrick skin type scale (Types I - VI)
Is willing and able to adhere to all study requirements, including accurate completion of VAS and questionnaires at the required time points, and is willing and able to travel to investigator's site to attend all required visits
Is able to understand the study plan, its conditions, the therapy goals and expected outcomes

Exclusion Criteria

To be eligible for inclusion into this study, the patient must not meet any of the following criteria prior to enrollment:

General:

Is participating in another clinical study at time of this study, or has participated in another study within the 30 days prior to signing the informed consent form
Is pregnant or breast-feeding
Is a sexually active female of childbearing potential and is not using a medically approved form of contraception
Has moderate or severe arterial hypertension (WHO/ISH grade 2 or higher; systolic BP ≥ 160 and/or a diastolic BP ≥ 100), a history of stroke, myocardial infarction, angina pectoris, arteriosclerotic vascular disease (ASVD), or peripheral vascular disease, or (severe) congestive heart failure
Is in poor general health
Is an employee of the investigational site directly affiliated with this study and/or their immediate family members; an employee of the sponsor or the CRO

Back Pain Related:

Has had any failed back surgery, or has had any surgery to torso, head or back within the previous 8 weeks
Had an acute dislocation or fracture within the previous 8 weeks
Has a degenerative central nervous system disease such as Multiple Sclerosis or Parkinson's disease; or a spinal stenosis that contributes to or is the cause of back pain; or Cauda equina syndrome, or other neurological symptoms indicating neuropathy
Has any sensory deprivation or diagnosis of shingles or postherpetic neuralgia (specifically in mid-trunk region)
Has wide spread pain
Has any inflammatory disease that causes pain or any other chronic disease or infection known to cause pain (e.g. spondyloarthropathy, rheumatoid arthritis, Lupus erythematodes, Lyme borreliosis, etc.)
Has schizophrenia, borderline syndrome or severe depression
Has or has had cancer
Has a history of severe osteoporosis (T score of 2.5 and a history of 1 or more bone fractures), or another severe bone disease
Is unwilling to abstain from other non-drug back pain treatments, such as massage, sauna, transcutaneous electrical nerve stimulation, etc., for the duration of the trial
Is unwilling to abstain from use of pain medication other than those recommended on steps 1 and 2 of the WHO Analgesic Ladder for the duration of the trial

Treatment Related:

Has a known sun allergy, or known allergy to any device related material
Uses steroids or any photosensitizing medication
Has any known disease or idiopathic dermatosis such as porphyria, polymorphic light eruption, chronic actinic dermatitis, actinic prurigo or solar urticaria that causes photosensitivity
Has a skin pathology, tattoo etc., or skin disease such as local infection, psoriasis, eczema etc. in the treatment area
Has any anatomical pathology or other limitation that would prevent successful placement of the device
Has an implanted medical device (screw, etc.) in or near the treatment area or an active implantable medical device such as cardiac pacemaker, defibrillator, neurostimulator, cochlear implant, active drug administration device anywhere in the body
Is unwilling to abstain from sunbathing or use of tanning lights for the duration of the trial
Is in the process of seeking early retirement, or is engaged in outstanding litigation involving back pain

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Pain Relief Patch	Pain Relief Patch	Pain Relief Patch: Light wavelength 453 ± 7 nm, maximum 42 ± 6 mW/cm2 and average 20 ± 1 mW/cm², 30 minutes
Control PRP device	Control PRP device	Control PRP device: Light wavelength 531 ± 7 nm, maximum 0.4 ± 0.1 mW/cm² and average 0.2 ± 0.05 mW/cm², light on for 5 seconds, device worn for 30 minutes

Primary Outcome Measures

Name	Time	Method
Change From Baseline (Mean of Three Measurements at Screening, Prior to Treatment Visit 1 and Treatment Visit 1 Pretreatment) in the Average Visual Analog Scale (VAS) Pain Intensity Over the 5 Treatment Days	Baseline (Visit 1/day -7, at home and Visit 2/day +1), Treatment (Visits 2-6 post treatment/days +1 to +14)	Pain intensity scored on a 10.0 cm VAS with the endpoints 0 = no pain; 10 = worst pain imaginable

Secondary Outcome Measures

Name	Time	Method
Change From Baseline in Roland-Morris Disability Questionnaire (RMDQ) at Visit 5	Baseline (days -7 to +1) to Treatment 5 (day +14)	The RMDQ is a 24 list of yes/no questions about the effects of back pain on the participants daily activities. Each positive answer is a point; maximum total score = 24.
Change From Baseline in VAS Pain Intensity at Follow up	Baseline (day -7 to 1) to Follow-up (up to day +42)
Change From Treatment in VAS Pain Intensity at Follow up	Treatment (day +1 to +14) to Follow-up (up to day +42)
Change From Baseline in RMDQ at Follow up	Baseline (days -7 to +1) to Follow-up (up to day +42)
Change From Treatment in RMDQ at Follow up	Treatment (days +1 to +14) to Follow up (up to day +42)
Frequency, Severity, Nature and Duration of Adverse Events During the Whole Duration of the Study	Baseline (days -7 to -1) to Follow up (up to day +42)	Adverse events will be assessed using descriptive statistical methods and compared between treatment arms.
Vital Sign Parameters	Baseline (days -7 to -1) to Follow up (up to day +42)	Vital signs (blood pressure and pulse)will be assessed at each visit and changes from baseline compared between the treatment groups
Changes From Baseline in Skin Condition	Baseline (days -7 to -1) to Follow up (up to day +42)	Skin condition (erythema and hyperpigmentation as measured with the MX-18) and appearance (recorded with Polaroid photos) will be assessed once each at baseline and follow up, and before and after each treatment. The changes from baseline will be analysed using descriptive statistics and the two treatment arms compared.
Average Visual Analog Scale Pain Relief Over 5 Treatments	5 treatments (days +1 to +14)	The average pain relief scored on a 10.0 cm VAS pain relief scale (endpoints 0 = no pain, 10 = no relief

Trial Locations

Locations (3): Pain Therapy Section, Dept of Orthopedic Surgery and Traumatology, University Hosp Heidelberg
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Heidelberg, Germany
University Medical Care Center Mannheim, Dept of Anaesthesiology and Surgical Care Medicine
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Mannheim, Germany
Clinic for Anaesthesiology and Supra-regional Center of Pain Therapy and Palliative Care, University Hosp Heidelberg
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Heidelberg, Germany