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Photobiomodulation Therapy to Reduce Pain and Inflammation in Patients With Gonarthrosis

Primary Purpose

Osteoarthritis, Gonarthrosis

Status
Not yet recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Photomodulation Therapy with the Light-Aid system
Control
Sponsored by
D'Or Institute for Research and Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis focused on measuring photobiomodulation, gonarthrosis, analgesia

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients of both sexes, aged between 50 and 75 years; Uni or bilateral symptomatic gonarthrosis grades II or III according to the Kellgren-Lawrence classification confirmed on radiographs with weight bearing in anteroposterior, lateral and axial patella. When the disease is bilateral, the knee indicated by the patient as being the most symptomatic will be included; Complaint of knee pain ≥4 on the Visual Analogue Scale at the time of inclusion in the study; Able to walk independently, with or without walking aids; Cognitive ability to answer questionnaires and perform physical tests; Agreement to participate in the study by signing the Free and Informed Consent Form (TCLE). Exclusion Criteria: Diagnosis of active malignancy except basal cell carcinoma (BCC); Diseases or neurological conditions that compromise the ability to perform the physical tests; Epilepsy; Skin lesions on the lower limb, close to the TFBM application site; Tattoos on the lower limb, close to the TFBM application site; Unicompartmental or total knee arthroplasty in the knee included in the study; History of direct trauma to the knee included in the study within the last six months; Active systemic inflammatory disease; Rheumatological diseases; Any previous procedure with an intra-articular approach to the knee in the last six months; Anticipation of adopting another form of treatment during the study period, including arthroplasty; Patients undergoing knee shock wave treatment in the knee included in the study; Absence, inability or refusal to sign the informed consent form.

Sites / Locations

  • Hospital Glória D'Or

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

FBM

Control

Arm Description

volunteers who will receive adjuvant photobiomodulation therapy (n=119)

volunteers who will receive placebo treatment with inert light (n=119)

Outcomes

Primary Outcome Measures

Change of knee pain scale by at least 20% in the FBM group assessed using the Visual Analog Scale (VAS).
The Visual Analogue Scale (VAS) evaluation is an instrument uses a scale of 0-10 to grade pain intensity, where 0 represents no pain and 10 the worst imaginable pain. The VAS will be applied daily until the 5th week of treatment and weekly from the sixth week to three months after treatment, through an online form sent daily to the patient via cell phone using an integrated application to the RedCap system or similar.

Secondary Outcome Measures

Full Information

First Posted
July 27, 2023
Last Updated
August 18, 2023
Sponsor
D'Or Institute for Research and Education
Collaborators
TERGOS PESQUISA E ENSINO S.A
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1. Study Identification

Unique Protocol Identification Number
NCT05975957
Brief Title
Photobiomodulation Therapy to Reduce Pain and Inflammation in Patients With Gonarthrosis
Official Title
Photobiomodulation Therapy to Reduce Pain and Inflammation in Patients With Gonarthrosis: a Multicenter Randomized, Double-blind, Placebo-controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 15, 2023 (Anticipated)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
August 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
D'Or Institute for Research and Education
Collaborators
TERGOS PESQUISA E ENSINO S.A

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Osteoarthritis (OA) is one of the main causes of chronic pain and physical disability, which directly impacts the quality of life of patients. The prevalence of OA among adults over 60 years of age is approximately 13% in women and 10% in men. Knee OA (gonarthrosis) has as main risk factors, in addition to age, female gender and obesity. Pharmacological treatment of gonarthrosis is based on approaches to reduce symptoms and/or pain, with joint replacement (arthroplasty) being reserved for more advanced forms of the disease. In general, currently available treatments have only moderate effects and low satisfaction rates among patients. Photobiomodulation Therapy (TFBM) has been used for at least 50 years by health professionals to treat a variety of clinical conditions, especially those associated with chronic pain. TFBM is a treatment using a non-ionizing light source such as Low Intensity Laser (LBI) or Light Emitting Diodes (LED), with near-infrared wavelengths. The aim of this study is to evaluate the intensity of knee pain in the short and medium term after photobiomodulation therapy in patients with gonarthrosis. In this multicenter, randomized, placebo-controlled, double-blind clinical trial, 238 volunteers with gonarthrosis grades II and III according to the Kellgren-Lawrence classification will be recruited to be administered adjuvant treatment with TFBM. The TFBM will be performed in the knee region, twice a week, for five weeks, totaling 10 sessions. Volunteers will be allocated in the intervention group (n=119) or in the placebo group, which will be treated with 10 sessions of inert light (n=119). The hypothesis is that the photobiomodulation therapy will have a positive impact, in the short and medium term, on improving pain, functionality and quality of life of patients with symptomatic gonarthrosis.
Detailed Description
Osteoarthritis (OA) is one of the main causes of chronic pain and physical disability, which directly impacts the quality of life of patients. The prevalence of OA among adults over 60 years of age is approximately 13% in women and 10% in men. Knee OA (gonarthrosis) has as main risk factors, in addition to age, female gender and obesity. It can involve all three compartments of the knee and is clinically characterized by pain and progressive impairment of cartilage, bone, synovial membrane and ligaments. Pharmacological treatment of gonarthrosis is based on approaches to reduce symptoms and/or pain, with joint replacement (arthroplasty) being reserved for more advanced forms of the disease. In general, currently available treatments have only moderate effects and low satisfaction rates among patients. Photobiomodulation Therapy (TFBM) has been used for at least 50 years by health professionals to treat a variety of clinical conditions, especially those associated with chronic pain. TFBM is a treatment using a non-ionizing light source such as Low Intensity Laser (LBI) or Light Emitting Diodes (LED), with near-infrared wavelengths. The technique does not emit heat, is painless and non-invasive and does not have significant side effects, and can be used as an adjuvant therapy to control pain associated with gonarthrosis. The aim of this study is to evaluate the intensity of knee pain in the short and medium term after photobiomodulation therapy in patients with gonarthrosis. In this multicenter, randomized, placebo-controlled, double-blind clinical trial, 238 volunteers with gonarthrosis grades II and III according to the Kellgren-Lawrence classification will be recruited to be administered adjuvant treatment with TFBM. The TFBM will be performed in the knee region, twice a week, for five weeks, totaling 10 sessions. Volunteers will be allocated in the intervention group (n=119) or in the placebo group, which will be treated with 10 sessions of inert light (n=119). The evaluations will be made before and after TFBM or placebo and will consist of (i) measurement of pain intensity through the application of questionnaires; (ii) verify the functional mobility of the knee joint and the muscle strength of the lower limb through physical tests; (iii) evaluate the quality of life and levels of anxiety and depression through the application of questionnaires; and (iv) record the consumption of medication for analgesic purposes and the frequency of physical therapy during the trial period. The hypothesis is that the photobiomodulation therapy will have a positive impact, in the short and medium term, on improving pain, functionality and quality of life of patients with symptomatic gonarthrosis. It is also expected to observe a reduction in pain on the Visual Analog Scale of more than 20% after 10 treatment sessions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Gonarthrosis
Keywords
photobiomodulation, gonarthrosis, analgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, multicenter randomized, double-blind, placebo-controlled clinical trial.
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
238 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FBM
Arm Type
Experimental
Arm Description
volunteers who will receive adjuvant photobiomodulation therapy (n=119)
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
volunteers who will receive placebo treatment with inert light (n=119)
Intervention Type
Device
Intervention Name(s)
Photomodulation Therapy with the Light-Aid system
Intervention Description
Patients in the intervention group (FBM) will be submitted to 10 treatment sessions (twice a week/five weeks) with the Light-Aid system (Bright Photomedicine, SP, Brazil), operated in continuous mode, with 100 LEDs of 850nm wave per tip, with application time varying from 4 to 8 minutes. Irradiation parameters will be customized based on pain intensity, skin phototype and Body Mass Index (BMI).
Intervention Type
Device
Intervention Name(s)
Control
Intervention Description
Patients in the placebo group will undergo the same therapeutic protocol as the FBM group using a device with the same appearance as the Light-Aid System, but with inert light emission. In both groups, the treatment will be administered in contact with the skin over the knee, with the patient positioned in dorsal decubitus. The three tips of the device will be positioned horizontally over the anterior region of the knee with the central tip over the patella.
Primary Outcome Measure Information:
Title
Change of knee pain scale by at least 20% in the FBM group assessed using the Visual Analog Scale (VAS).
Description
The Visual Analogue Scale (VAS) evaluation is an instrument uses a scale of 0-10 to grade pain intensity, where 0 represents no pain and 10 the worst imaginable pain. The VAS will be applied daily until the 5th week of treatment and weekly from the sixth week to three months after treatment, through an online form sent daily to the patient via cell phone using an integrated application to the RedCap system or similar.
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of both sexes, aged between 50 and 75 years; Uni or bilateral symptomatic gonarthrosis grades II or III according to the Kellgren-Lawrence classification confirmed on radiographs with weight bearing in anteroposterior, lateral and axial patella. When the disease is bilateral, the knee indicated by the patient as being the most symptomatic will be included; Complaint of knee pain ≥4 on the Visual Analogue Scale at the time of inclusion in the study; Able to walk independently, with or without walking aids; Cognitive ability to answer questionnaires and perform physical tests; Agreement to participate in the study by signing the Free and Informed Consent Form (TCLE). Exclusion Criteria: Diagnosis of active malignancy except basal cell carcinoma (BCC); Diseases or neurological conditions that compromise the ability to perform the physical tests; Epilepsy; Skin lesions on the lower limb, close to the TFBM application site; Tattoos on the lower limb, close to the TFBM application site; Unicompartmental or total knee arthroplasty in the knee included in the study; History of direct trauma to the knee included in the study within the last six months; Active systemic inflammatory disease; Rheumatological diseases; Any previous procedure with an intra-articular approach to the knee in the last six months; Anticipation of adopting another form of treatment during the study period, including arthroplasty; Patients undergoing knee shock wave treatment in the knee included in the study; Absence, inability or refusal to sign the informed consent form.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Veronica Vianna, Ph.D
Phone
+5521995888008
Email
veronica.vianna@rededor.org
First Name & Middle Initial & Last Name or Official Title & Degree
Maria EL Duarte, Ph.D
Phone
+5521981111294
Email
maria.leite@idor.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Veronica Vianna
Organizational Affiliation
Instituto D'Or de Pesquisa e Ensino
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Glória D'Or
City
Rio De Janeiro
ZIP/Postal Code
22211-230
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria EL Duarte
Phone
+5521981111294
Email
maria.leite@idor.org

12. IPD Sharing Statement

Plan to Share IPD
No
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Photobiomodulation Therapy to Reduce Pain and Inflammation in Patients With Gonarthrosis

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