W.l.gore & Associates

This study looks at a device that closes a small hole in the heart (called PFO) to help prevent strokes in people who have had a stroke with no clear cause. About 300 people in Japan will be followed for 12 months after the procedure. The main goal is to see if the device safely …

This study tests a new stent device (GORE EXCLUDER TAMBE) to treat thoracoabdominal and pararenal aortic aneurysms—dangerous bulges in the main artery. About 102 to 202 participants will receive the stent via a minimally invasive procedure. The goal is to see if the device can sa…

This early study tests a new device called the GORE Glaucoma Drainage Implant in 30 adults with primary open-angle glaucoma that eye drops cannot control or who are at high risk of scarring from standard surgery. The goal is to see if the implant safely lowers eye pressure by at …

This study looks at a special device called the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis for treating aneurysms in the chest and belly area. These aneurysms are bulges in the main blood vessel that can burst if not treated. The device is placed inside the blood vessel…

This study tests a device called the GORE Ascending Stent Graft to treat serious conditions of the ascending aorta, such as aneurysms (bulging blood vessels), dissections (tears), and ulcers. The goal is to repair these lesions using a less invasive procedure instead of open-hear…

This study follows 320 people who had ventral or incisional hernia repair using GORE SYNECOR mesh. Researchers track hernia recurrence, infections, and other complications over 5 years. The goal is to see how well the mesh works in real-world use, not to cure the hernia but to im…

This study tracks 300 people who receive a special stent graft to treat aneurysms in the abdomen or chest area. The goal is to confirm the device works well and is safe in everyday medical practice. Participants are followed for a year to check for complications like leaks, block…

This study tests a special stent (a small mesh tube) to treat blockages in the large vein that returns blood from the lower body to the heart. About 136 adults with symptoms like leg swelling, pain, or ulcers will receive the stent and be followed for a year. The goal is to see i…

This study tests a new device (GORE TAG TBE) to treat weak spots or tears in the main artery of the chest. It involves 250 adults who need repair in a specific area (Zone 2). The device is placed through a small tube in a blood vessel, avoiding open surgery, and aims to safely se…

This study is testing a new device called the GORE PV1 to replace the pulmonary valve and rebuild the right ventricular outflow tract in people with congenital heart defects. The device is designed to improve blood flow from the heart to the lungs. The study includes 15 participa…

This study is a large registry that collects real-world information on how well Gore aortic stent grafts work and what complications may occur. It follows about 4,600 people who need a minimally invasive repair of an aortic aneurysm or other aortic condition. The goal is to track…

This study is a registry that collects safety and performance data on the GORE® VIABAHN® VBX Stent Graft when used in peripheral vessels. It involves 280 adults who need this device to treat peripheral vascular disease. The goal is to see how well the stent graft works and if the…

This study collects information from over 600 patients who have already received the GORE VIABAHN stent-graft for conditions like peripheral artery disease, aneurysms, or trauma. The goal is to track how often serious device-related problems occur in everyday medical practice. No…