LOS ANGELES and ST. LOUIS, Nov. 3, 2016 /PRNewswire/ -- EndoStim, Inc., announced that the first patient has been implanted with the EndoStim device in the LESS GERD trial, at the University of Southern California. The results from the trial will support EndoStim's premarket approval application to the U.S. Food and Drug Administration (FDA).
The LESS GERD trial will include a minimum of 110 subjects implanted with the EndoStim device at up to 30 sites in the United States and Europe. The trial is a multicenter, randomized, double-blind, sham-controlled pivotal trial designed to evaluate the safety and efficacy of the EndoStim Lower Esophageal Sphincter (LES) Stimulation System in patients with gastro-esophageal reflux disease (GERD) who experience symptoms despite taking high-dose proton pump inhibitor (PPI) medications. The lead investigators of the LESS GERD trial are: Nicholas Shaheen, MD, MPH, Professor of Medicine and Chief of Gastroenterology and Hepatology at the University of North Carolina, Chapel Hill; and John Hunter, MD, Mackenzie Professor of Surgery and Interim Dean at Oregon Health & Science University School of Medicine. "Published international data suggest that the EndoStim system can successfully control symptoms and abnormal acid exposure in the esophagus and significantly improve patients' quality of life with minimal side effects," commented Dr. Shaheen. "This is why we anxiously await the outcomes of the LESS GERD trial." "The less invasive and less disruptive design of the EndoStim technology has the potential to change the care of the patient with medication-resistant gastroesophageal reflux," said Dr. Hunter. "I'm thrilled to have the opportunity to lead this trial along with a renowned group of investigators."