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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Hard tissue enlargement of 2 or more of 10 selected joints
Hard tissue enlargement of 2 or more distal interphalangeal (DIP) joints
Must not have
Known diagnosis of another type of arthritis: rheumatoid, psoriatic, crystalline, inflammatory bowel associated arthritis
Surgery within the past 6 weeks
Timeline
Screening 3 weeks
Treatment Varies
Follow Up visit 7 (week 12)
Summary
This trial is testing a special light therapy called Low-Level Laser Therapy (LLLT) to see if it helps reduce pain and improve function in adults with hand osteoarthritis. The laser works by warming up tissues to relieve pain and improve blood flow. Low-Level Laser Therapy (LLLT) has been used in various fields to promote tissue repair, reduce inflammation, and relieve pain.
Who is the study for?
This trial is for Active Duty and DoD Beneficiaries over 18 with hand osteoarthritis, showing specific joint enlargements and deformities but not more than three swollen joints. Excluded are those who've had recent surgery or fractures, pregnant individuals, patients treated with LLLT in the past 12 weeks, or have other arthritis types.
What is being tested?
The study tests the Phoenix Thera-Lase System's effectiveness on hand osteoarthritis pain and function against a sham (placebo) device. Participants will receive weekly treatments for six weeks and have their pain and hand functionality assessed using DVPRS and DASH questionnaires.
What are the potential side effects?
Since this trial involves a low-level laser therapy system versus a sham treatment, side effects may be minimal to none. However, potential mild side effects could include local discomfort or skin irritation at the site of application.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have swelling in 2 or more of my major joints.
Select...
I have swelling in two or more of my finger joints closest to the nails.
Select...
I have less than 3 swollen finger joints.
Select...
One of my joints is deformed.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have been diagnosed with a specific type of arthritis (rheumatoid, psoriatic, etc.).
Select...
I have had surgery in the last 6 weeks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ visit 7 (week 12)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~visit 7 (week 12)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Pain
Hand
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Group 1 (LLLT)Experimental Treatment1 Intervention
Group 1: Low level laser therapy (LLLT) using Phoenix Thera-lase device (74 Watts, 1275 nm wavelength) for 6 minutes affected per hand.
The protocol for each group will involve one minute of LLLT over each of the following treatment zones: dorsal fingers and thumb, dorsal metacarpals, dorsal wrist, palmar fingers and thumb, palmar metacarpals, palmar wrist for a total of 6 minutes affected on each hand. The LLLT device will be held approximately 12 inches from the skin surface.
Group II: Group 2 (LLLT Sham)Placebo Group1 Intervention
Group 2: Sham LLLT using the Phoenix Thera-lase device with the guide light on but without emitting laser photons for 6 minutes affected per hand.
The protocol for each group will involve one minute of sham LLLT over each of the following treatment zones: dorsal fingers and thumb, dorsal metacarpals, dorsal wrist, palmar fingers and thumb, palmar metacarpals, palmar wrist for a total of 6 minutes affected on each hand. The LLLT device will be held approximately 12 inches from the skin surface.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Low-Level Laser Therapy (LLLT) reduces pain and inflammation and promotes tissue repair and regeneration by using specific wavelengths of light to penetrate tissues, which can stimulate cellular activity and enhance blood flow. Topical nitroglycerin may improve tendon healing by stimulating collagen synthesis through the release of nitric oxide.
Ultrasound-guided percutaneous needle tenotomy involves using a needle to break up tendinotic tissue and calcifications, potentially stimulating an inflammatory response that promotes healing. Understanding these mechanisms helps pain management patients and their doctors choose the most appropriate treatment based on the underlying causes of their pain and the specific benefits of each therapy.
Preliminary clinical experience of low-level laser therapy for the treatment of canine osteoarthritis-associated pain: A retrospective investigation on 17 dogs.Photobiomodulation therapy by NIR laser in persistent pain: an analytical study in the rat.The Role of Descending Modulation in Manual Therapy and Its Analgesic Implications: A Narrative Review.
Preliminary clinical experience of low-level laser therapy for the treatment of canine osteoarthritis-associated pain: A retrospective investigation on 17 dogs.Photobiomodulation therapy by NIR laser in persistent pain: an analytical study in the rat.The Role of Descending Modulation in Manual Therapy and Its Analgesic Implications: A Narrative Review.
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Who is running the clinical trial?
David MossLead Sponsor
4 Previous Clinical Trials
656 Total Patients Enrolled
mallory kruegerLead Sponsor
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been diagnosed with a specific type of arthritis (rheumatoid, psoriatic, etc.).I have had surgery in the last 6 weeks.I have not had low-level laser therapy in the last 3 months.I broke my hand in the last 6 weeks.I experience hand pain, aching, or stiffness.I have swelling in 2 or more of my major joints.I am over 18 and either active duty or a DoD beneficiary.I have swelling in two or more of my finger joints closest to the nails.I have less than 3 swollen finger joints.One of my joints is deformed.
Research Study Groups:
This trial has the following groups:- Group 1: Group 1 (LLLT)
- Group 2: Group 2 (LLLT Sham)
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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