Canon Medical Signals Its Support for a Multicenter Ultrasound Liver Evaluation and Assessment Study

Canon Medical announced today its support for the iLEAD (innovative Liver, Elasticity, Attenuation and Dispersion) study, an international multicenter study aiming to evaluate quantitative ultrasound imaging tools against liver biopsy (the current clinical gold standard), available on the Aplio Liver Package for the assessment of Steatosis, Fibrosis, and Inflammation in the clinical environment.

This Multicenter study is focusing on the assessment of NASH (Non-Alcoholic SteatoHepatitis) using non-invasive innovative ultrasound liver imaging techniques against the current gold standard of liver biopsy. Researchers from China, Japan, South Korea, USA and Europe, aim to recruit over 200 patients for the study and to compare their results. Researchers believe that the non-invasive ultrasound diagnostics can provide a faster, safer, and more readily available assessment of NASH that may benefit patients by earlier detection, treatment and follow up.

The Aplio system now boasts three separate technologies and an integrated multi-parametric reporting capability that brings quantifiable imaging of the liver into the daily routine.

  • Shear Wave Elastography (SWE)
  • Shear Wave Dispersion (SWD)
  • Attenuation Imaging (ATI)

These tools include safe, non-invasive, robust, and reproducible quantitative assessment of Liver.

The global burden of liver disease, along with its significant individual, community and financial implications, has driven ultrasound development of non-invasive, safe tools. These can be utilized to diagnose and follow up patients at risk of steatosis, with implications for not only severe liver disease, cardiovascular disease and diabetes.

Aplio i-series, first launched in 2016, is widely used for premium performance abdominal imaging. The development of non-invasive assessment and staging tools for liver disease has the potential to reach into the community to provide quantitative health data that supports the management of liver disease, regardless of population location.

“This is an exciting step in the validation of non-invasive tools for the assessment and management of liver disease,” said representative researcher, Prof. Fuminori Moriyasu, Professor & Director, Center for Cancer Ablation Therapy, International University of Health and Welfare, Sanno Hospital, Tokyo, Japan.

“The liver tools provided by the Aplio result from over 50 years of technological development, knowledge and expertise, combined with strong collaboration with global clinical partners,” said Akihiro Sano, General Manager, Ultrasound, Canon Medical.

The Multicenter study is targeting RSNA 2022 to present its findings; with interim findings released as appropriate.

Aplio is a trademark of Canon Medical Systems Corporation.

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.”