Covid-19 Recovery Photobiomodulation Device – Vielight Inc https://www.vielight.com Advancing brain photobiomodulation technology. Fri, 05 Sep 2025 15:04:12 +0000 en-US hourly 1 https://wordpress.org/?v=6.8.3 https://www.vielight.com/wp-content/uploads/2025/06/cropped-Vielight-Favicon-General-1-32x32.webp Covid-19 Recovery Photobiomodulation Device – Vielight Inc https://www.vielight.com 32 32 Vielight RX Plus | Medical Device License Expansion! (Upper Respiratory Viral Symptom Recovery) https://www.vielight.com/blog/vielight-rx-plus-medical-device-license-expansion-upper-respiratory-viral-symptom-recovery/ Wed, 12 Jun 2024 19:56:31 +0000 https://www.vielight.com/?p=37807

World’s First PBM Medical Device License for Upper Respiratory Symptoms Recovery from Viral Infections!

We are honored to announce that Health Canada has expanded our RX-Plus medical device license to encompass the recovery of upper respiratory symptoms in all viral infections, extending beyond Covid-19!

To date, the RX Plus is the only PBM device supported by statistically significant results in a large (n=294) clinical trial for accelerated recovery from viral infection.

YouTube player

Stay tuned for the journal publication, which goes over the mechanisms of how NIR energy can modulate and improve immune responses and accelerate recovery against respiratory-based viral symptoms.

Find our license here: Link 

To learn more about our systemic technology: Link

Vielight is a fully-licensed medical device manufacturer (ISO13485 and MDSAP certified).

The post Vielight RX Plus | Medical Device License Expansion! (Upper Respiratory Viral Symptom Recovery) appeared first on Vielight Inc.

]]>
Accelerated Viral Recovery Major Clinical Trial Results | 294 Participants nonadult
Viral and Immunity Recovery Results | Vielight RX-Plus Major Clinical Trial (n=294) | Health Canada Medical Device License https://www.vielight.com/blog/viral-and-immunity-recovery-results-vielight-rx-plus-major-clinical-trial-n228-medical-device-license/ Wed, 03 Jan 2024 20:36:27 +0000 https://www.vielight.com/?p=41358

These results are based on a major viral recovery clinical trial (n=294) conducted with the Vielight RX-Plus 4

The Vielight RX-Plus is the only PBM device supported by published clinical results for viral recovery and inflammatory-based immunity (September 2024).

Health Canada medical device license indication: “The Vielight RX Plus is intended to accelerate the recovery of upper respiratory symptoms in viral infections, such as COVID-19” | Health Canada Medical Device License

Introduction

Although the Covid-19 pandemic has officially ended worldwide, thousands of people continue to be hospitalized weekly due to Covid-19 and upper respiratory viral infections. Athletes and elderly individuals are both particularly vulnerable to upper respiratory viral infections, though in different ways.

In elderly individuals, weakened immune responses and pre-existing health conditions can make respiratory infections more severe, leading to complications such as pneumonia or hospitalization.

For athletes, these infections can impair respiratory function, reduce oxygen intake, and hinder physical performance, often delaying recovery and training. Intense physical activity can also temporarily suppress the immune system, increasing susceptibility to infections.

This large-scale clinical trial (n=294) studied the affects of systemic and intranasal photobiomodulation on viral recovery speed and efficacy.

Introduction

This first-of-its-kind PBM major clinical trial (n=294) with the Vielight RX-Plus (Vielight X-Plus 4 equivalent) examined the efficacy of photobiomodulation (PBM) in treating acute COVID-19 infections.

The primary focus was on recovery speed in patients with moderate-to-severe symptoms. Patients with symptom durations of 0–7 days experienced significantly faster recovery when treated with PBM and standard care (SOC) compared to SOC alone. However, those with 8–12 days of symptoms did not show significant improvement.

Recruitment

Recruitment began in September 2020, with 701 adults who tested positive for COVID-19 assessed for eligibility. Of these, 407 did not meet the inclusion/exclusion criteria: 406 participants either had severity scores outside the required 4-7 range on the WURSS-44 scale or were outside the age range of 18-65, while one couldn’t complete forms in English. This left 294 eligible participants. Recruitment ended on July 5, 2021, due to the availability of monoclonal antibodies, declining interest, and sufficient numbers for statistical power, after which the datasets were locked.

Results summary

This study evaluated the effectiveness of photobiomodulation (PBM) therapy, specifically the Vielight RX Plus, in accelerating recovery from COVID-19 for non-hospitalized patients with moderate-to-severe symptoms. In patients experiencing symptoms for 0–7 days, PBM significantly reduced recovery time compared to standard of care (SOC) alone. However, in those with longer symptom durations (8–12 days), PBM did not produce a statistically significant improvement.

PBM was particularly effective in alleviating respiratory symptoms and reducing adverse effects like tachycardia and dysgeusia. It also contributed to a quicker recovery in specific symptoms such as headache, chest congestion, and body aches for patients in the 0–7 day symptom group. In contrast, the 8–12 day group showed slower recovery from fatigue and other energy-related symptoms, though they did experience milder symptom severity for some issues.

The study attributes the benefits of PBM to its anti-inflammatory effects, which have been linked to reduced cytokine levels in past research.

Recruitment Structure

Figure 1 – Flowchart of participants through each stage of the randomized trial.396 LIM ET AL.

Kaplan–Meier Curve of Primary Outcome

Figure 2 – Kaplan–Meier Curve of Primary Outcome. Symptoms duration of 0–7 days at Baseline. “How Sick Do You Feel Today?” (WURSS-44 Q1). This figure shows the probability of not recovering from the WURSS-44 Q1 symptom of “How sick do you feel today?”. It represents the outcome for the stratified group with symptom duration of 0–7 days at Baseline (0–5 days on Enrollment).

Secondary Outcomes

Table 3 – Secondary Outcomes of Patients by Symptom Duration Strata

The post Viral and Immunity Recovery Results | Vielight RX-Plus Major Clinical Trial (n=294) | Health Canada Medical Device License appeared first on Vielight Inc.

]]>
Vielight Inc. Receives Health Canada Approval for Treatment of Covid-19 with Near Infrared Device Technology https://www.vielight.com/blog/vielight-inc-receives-health-canada-approval-for-treatment-of-covid-19-with-near-infrared-device-technology/ Thu, 25 May 2023 13:26:58 +0000 https://www.vielight.com/?p=31455

Approval from Canada’s Top Federal Health Agency Followed Positive Clinical Trial Results

We are honored to announce that the Vielight RX Plus device has received medical device approval from Health Canada!

We conducted an n=295 clinical trial for Covid-19 recovery for which the results were statistically significant.

This represents two historic milestones:

  1. The RX Plus is the first medical device to be approved for the treatment of COVID-19 infection.
  2. The RX Plus is the first non-invasive photobiomodulation (PBM) technology to be approved for a major indication.

The RX Plus combines our patented red and near-infrared light technology to accelerate the recovery of adults with COVID-19. We designed it to be non-invasive, portable, and lightweight to meet the needs of those who prefer to recover at home or on-the-go.

The effects of Photobiomodulation on Immunity. 

(The text below is based on an article from Liebert A, Bicknell B, Markman W, Kiat H. A Potential Role for Photobiomodulation Therapy in Disease Treatment and Prevention in the Era of COVID-19. Aging Dis. 2020 Dec 1;11(6):1352-1362. doi: 10.14336/AD.2020.0901. PMID: 33269093; PMCID: PMC7673843)

PBM appears to exert pluripotent effects in the modulation of inflammation and immunity []. Many studies have demonstrated that PBM modulates inflammation by reducing the pro-inflammatory cytokines (such as IL-1β, IL-6, IL-8, TNF-α) and other inflammatory markers released from activated inflammatory cells, while increasing the anti-inflammatory cytokines (IL-10) []. The immuno-modulatory effect of PBM on cytokines regulation and the complement cascade occurs via the POMC pathway, involving regulation of the hypothalamic pituitary axis through the direct modulation of the POMC/melanocortin signalling pathway including a-MSH, a potent anti-inflammatory molecule. The POMC pathway is regulated by PBM [], which in turn modulates both ACTH and β-opioid, as well as, interestingly, ACE activity [].

One of the central effects of PBM on the immune response is via the modulation of neutrophil function [] by balancing neutrophil numbers, improving neutrophil efficiency and modulating the neutrophil extracellular trap formation []. Reducing over-accumulation of neutrophils is a major mechanism for the effect of PBM in reducing acute lung inflammation []. This is crucial in preventing the cytokine storm cascade in autoimmune diseases. PBM also modulates the ratio of M1 and M2 macrophage phenotypes, reducing pro-inflammatory cytokines and chemokines and increasing anti-inflammatory cytokines and thus balance the inflammatory process [].

These inflammatory changes facilitated by PBM have profound effects on many body processes. For example, PBM therapy has been shown to modulate peripheral blood mononuclear cells and CD4+ cells to reduce inflammatory effects in multiple sclerosis patients and healthy adults by increasing IL-10 and reducing IFN-γ []. PBM reduces the number of inflammatory cells, pro-inflammatory cytokines as well as fibrotic tissue in a mouse model of lung fibrosis []. Acute lung inflammation in rats is reduced with PBM to reduce oedema, neutrophil influx and TNF-α, while reducing IL-10 in rats [].

In an experimental model of induced acute peritonitis in rats, Yu and co-workers [] showed PBM resulted in lymphocyte proliferation and enhanced lymphocyte ATP synthesis compared to controls, and the 60-day survival rate of the PBM group was double that of the control group (p<0.001). Assis et al [] further demonstrated the immune modulation capability of PBM, with septic rats treated with PBM exhibiting lower IL-6 activity and decreased atrogin-1 and MuRF-1 immuno-expression (markers of sepsis related muscle catabolic states).

PBM causes mitogenic stimulation responsive lymphocyte proliferation and enhanced lymphocyte ATP synthesis [5]. A plausible mechanism for PBM induced lymphocytic proliferation is through the reaction of light with haemoglobin, resulting in oxygen radical production [6]. Indeed, in immunological cells, PBM induces production of reactive oxygen species, NO or interleukins most often, leading to an anti-inflammatory effect []. It is well documented that various immune response processes are highly dependent on cellular energy, the latter being depressed in sepsis and septic shock cases []. The mitochondria probably act as photo-acceptors for PBM and robustly reactivate cellular energy synthesis to re-establish ATP levels in a variety of cells including lymphocytes and macrophages, and through several pathways that trigger activation of nucleic acid synthesis and cellular proliferation [].

Reference

  • Liebert A, Bicknell B, Markman W, Kiat H. A Potential Role for Photobiomodulation Therapy in Disease Treatment and Prevention in the Era of COVID-19. Aging Dis. 2020 Dec 1;11(6):1352-1362. doi: 10.14336/AD.2020.0901. PMID: 33269093; PMCID: PMC7673843.

The post Vielight Inc. Receives Health Canada Approval for Treatment of Covid-19 with Near Infrared Device Technology appeared first on Vielight Inc.

]]>