VenoStent Embarks on Clinical Trial to Improve Success Rate of Vascular Surgery Outcomes

Successful enrollment in initial feasibility trial to support future regulatory submissions and provide better outcomes for patients with end-stage renal disease

VenoStent is a clinical-stage tissue engineering company developing tunable, bioabsorbable, smart polymer wraps to fundamentally transform the efficacy of the five million vascular surgeries performed each year, announces successful enrollment in its initial feasibility clinical trial.

The clinical trial is testing the safety and efficacy of its 3D-printed bioabsorbable wraps in humans, a new methodology to improve surgical outcomes for hemodialysis patients.

“We are very pleased to announce that we have successfully enrolled twenty end-stage renal disease patients in our initial feasibility study taking place in Asuncion, Paraguay,” says Tim Boire, CEO. “After years of development, we are confident that our bioabsorbable wrap technology can have a positive impact on the lives of patients that require hemodialysis to sustain life. This is a major milestone toward our mission to improve the quality and length of life for end-stage renal disease patients, as well as others needing vascular surgery.”

Feasibility Study

Enrollment was completed for the initial VenoStent Feasibility Study in Paraguay involving 20 end-stage renal disease patients that were referred for creation of an arteriovenous fistula—surgical connection of an artery to a vein in the arm—to enable hemodialysis treatments. The participants in the study are followed up for several months and the team has already seen highly encouraging safety and performance signals, which could indicate much greater clinical outcomes and quality of life for kidney disease patients when treated with the VenoStent SelfWrap® Bioabsorbable Perivascular Wrap technology.

Approximately 60% of the blood vessels used for dialysis, and 20% of the blood vessels used for quadruple bypass, fail within 12 months of the vascular surgery, risking the lives of 5 million patients every year. The reason for this 60% failure rate is that the vein is not accustomed to, nor equipped for, the high pressure, high flow arterial environment. The thin-walled vein expands, causing tearing of the protective inner lining of the vein. In response to this expansion and tearing, the cells inside the vein wall begin a repair process and migrate inward. This remodeling and cell growth response (also called neointimal hyperplasia) ultimately leads to reduction in, or complete blockage of, blood flow. VenoStent’s proprietary bioabsorbable scaffold goes around these blood vessels at the time of vascular surgery to aid in their “arterialization” process. To make its implantable smart polymer wraps, VenoStent utilizes advanced stereolithography fabrication with 3D printers supplied by Volumetric, a fellow Houston alum of the California-based accelerator Y Combinator.

 

SourceVenoStent

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.”
Exit mobile version