Medical Device News Magazine

Symposium on Advanced Wound Care: Regenative Labs to Present Its Groundbreaking Wharton’s Jelly Studies

About Medical Device News Magazine

About Medical Device News Magazine. We are a digital publication founded in 2008 located in the United States.

Advertise with Medical Device News Magazine! Join Our #1 Family of Advertisers!

We pride ourselves on being the best-kept secret when it comes to distributing your news! Our unique digital approach enables us to circulate your...

Regenative Labs (Regenative), a leading provider of regenerative medicine solutions, announced that it will present two scientific studies demonstrating the efficacy of Wharton’s jelly allografts in complicated post-surgical wounds and late-stage sacral decubitus ulcers at the Symposium on Advanced Wound Care (SAWC) conference.

Regenative’s first study showcases the successful use of its Wharton’s jelly flowable perinatal tissue allografts for a patient who experienced postoperative wound dehiscence after undergoing a lower body lift, breast reduction, and nipple-areolar transplant. The patient’s wound had failed to close after eight weeks of conservative treatment, but after receiving a single dose of Wharton’s jelly and twelve hyperbaric oxygen therapy visits, the wound healed entirely with 100 percent epithelialization overlying granulation tissue. The case study demonstrates the potential of Wharton’s jelly allografts in improving patient outcomes by offering an alternative to conventional treatment methods.

Regenative’s second study presents two patients with stage IV sacral decubitus ulcers. Both patients received six Wharton’s jelly applications and standard wound dressing during the study. The first patient with a ten-year-old wound experienced a 94 percent decrease in wound volume despite noncompliant at-home care. The second patient achieved a 100 percent decrease in wound volume compared to previous 30 months of failed conservative treatment. This study provides grounds for future research into the preventative application of Wharton’s jelly to stage II ulcers or earlier.

“We are excited to present these two groundbreaking studies at the SAWC conference,” said Tyler Barrett, CEO of Regenative Labs. “These results demonstrate the potential of Wharton’s jelly allografts in improving patient outcomes. We believe that these findings will have a significant impact on the field of regenerative medicine and wound care,” Barrett concluded.

Regenative Labs will present these studies at SAWC Spring | WHS, which will be held April 26–30 in National Harbor, Maryland. The 2023 event is co-located with the Diabetic Limb Salvage (DLS) conference to provide the latest education on the prevention and management of wound care, current scientific findings, and the most up-to-date limb salvage techniques.

For more information about the studies or to speak with one of its authors, please contact Regenative Labs on their website.

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Other News

Shoulder Innovations Further Strengthens IP Portfolio in Key Areas with Recent Patent Grants

"These recent grants further strengthen key patent families that are foundational to our technology, and we are pleased the USPTO continues to recognize our meaningful innovation in the shoulder arthroplasty segment," said Rob Ball, CEO of Shoulder Innovations. "This noteworthy expansion of our IP position represents the culmination of over 10 years of research and development, and we are proud of our team for their continued dedication to creating practical solutions for shoulder surgeons and advancing patient outcomes."

Radical Catheter Technologies Presents Analysis of Disruptive, Recently FDA-Cleared Endovascular Technology at the Society of NeuroInterventional Surgery 21st Annual Meeting

This new catheter, the first product commercialized from this novel technology platform, is designed to enable access to the blood vessels in the brain for both femoral and radial access. A multi-center analysis of this disruptive technology is being presented today at Society of NeuroInterventional Surgery 21st annual meeting. In addition, the Company confirmed the closing of a $20 million financing round led by NeuroTechnology Investors, which will be used to scale the company and expand the Radical platform notes Radical Catheter Technologies.

Rapid Medical™ Completes Initial Neurovascular Cases in the USA Following FDA Clearance of Its Active Access Solution

“With DRIVEWIRE, our design goal was to bring new levels of access and control to the interventional suite while improving best-in-class guidewires,” comments Giora Kornblau, Chief Technology Officer at Rapid Medical. “When physicians are looking for technologies that increase the clinical possibilities and safety for the patient, we want Rapid to be the first place they look.”