Non-Pharmaceutical Clinical Trial Starts Using Photobiomodulation to Treat Intubated COVID-19 Patients

May 27, 2020

Non-Pharmaceutical clinical trial started by researchers in Brazil using Multi Radiance Medical super pulsed laser therapy technology as an adjunctive means to improve critical care for COVID-19 patients is underway.

Approved by the Ministry of Health in Brazil, a group of international physicians and scientists are in the early stages of data collection utilizing Multi Radiance Medical’s handheld super pulsed laser therapy devices to improve the condition of patients.

The study, the first of its kind to utilize light therapy for COVID-19 patient recovery, will evaluate the respiratory muscle function and levels of inflammation during intubation. There is a profound effect seen following a brief exposure to multi-wavelength light on muscle fatigue.

Coordinated by Drs. Fabio Francio, Ernesto Leal-Junior, and Thiago DeMarchi, the trial aims to use low level laser therapy for general improvement of hospitalized COVID-19 patients in intensive care units by decreasing the length of hospitalization of these patients through improving ventilation and immune response, and decreasing inflammation.

Previous work done by Leal-Junior and his team at the Laboratory of Phototherapy and Innovative Technology (LaPIT) on human performance enhancement with light sparked interest in the researchers at the Hospital Tacchini located in Bento Gonçalves – RS (Brazil).

“Prior trials have successfully demonstrated improvement in lung function in chronic obstructive pulmonary disease (COPD) patients. The hospital contacted us due to the solid and robust outcomes published in many randomized clinical trials using Multi Radiance technology,” says Leal-Junior.

Multi Radiance has over 30 peer-reviewed, published studies validating its technology as safe and effective for pain relief and accelerated recovery. The company has a history of innovation, participating in trials and securing patents in fibromyalgia, neurology, ophthalmology, and now immunology with this new clinical trial.

“This pandemic has impacted us all greatly. Multi Radiance is excited to partake in a trial that could become a piece of the critical care solution for COVID-19 patients,” says Founder and CEO Max Kanarsky.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”