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Clare Medical of New Jersey reported in a recent study that its proprietary artificial intelligence (AI) tool that identifies elderly patients with a high probability of needing an emergency room (ER) visit or hospitalization within 30 days reduced these visits by 77 percent. Read More
Insulet has released pivotal trial extension data showing that its Omnipod 5 automated insulin delivery system continued to improve glycemic outcomes in young children over 12 months of use. Read More
New York-based DarioHealth reported positive results from several clinical trials of its digital therapeutics at the American Diabetes Association’s (ADA) 82nd Scientific Sessions in New Orleans, June 3-7. Read More
3DBio Therapeutics, a New York-based regenerative medicine company, and the Microtia-Congenital Ear Deformity Institute in San Antonio, Texas, have partnered to reconstruct a human ear using the company’s AuriNovo 3D-bioprinted implant. Read More
Helsinki, Finland-based Bioretec’s bioresorbable Activa IM-Nail was effective in treating pediatric forearm fractures in an ongoing postmarket study by European researchers. Read More
Orthofix Medical’s M6-C artificial cervical disc showed significant benefit over spinal fusion in data from a five-year clinical trial conducted under and FDA Investigational Device Exemption (IDE). Read More
Efforts to improve diversity in clinical research can be greatly improved when sponsors take a hard look at their current practices and protocols, work directly with sites and consider adding sites well-suited for the task, a new report from the Advanced Medical Technology Association (AdvaMed) advises. Read More
Verily Life Sciences’ investigational smartwatch has shown potential for monitoring Parkinson’s disease in home settings in a multiyear European study. Read More
Vibrant Gastro is touting positive results from a late-stage study of its drug-free treatment for adults with chronic idiopathic constipation (CIC). Read More
In a congressionally mandated report on diversity in clinical trials, the National Academies of Sciences, Engineering and Medicine (NASEM) recommends the FDA require sponsors to file an in-depth recruitment strategy, either before or with their investigational device exemption (IDE) applications, that details how they intend to make their trial population reflective of the disease or condition’s demographics. Read More
Abbott reported study findings for its TriClip tricuspid heart valve repair device at the annual European Association of Percutaneous Cardiovascular Interventions (EuroPCR) meeting being held this week in Paris, France. Read More
Patients whose feeding tubes were placed using Baltimore, Md.-based CoapTech’s PUMA-G bedside ultrasound imaging system had shorter hospital stays, according to researchers at the University of Maryland’s medical center. Read More