General Eligibility
Clinical Trials
Filter by enrollment status to find studies that may be right for you. We value your participation in advancing care for bladder control and incontinence.
Status: Active, Not Enrolling
The Restore study is evaluating therapies designed to improve bladder function and reduce symptoms associated with urinary incontinence. The study seeks to provide patients with additional treatment options and long-term symptom relief.
BlueWind Medical Restore
BlueWind Revi was crafted with the patient and the physicians who treat UUI in mind. This advanced implant design allows for the device to be miniature in size without the need for replacement surgeries for battery change, lead migration, or lead fracture. The innovative external wearable technology powers the implant for a patient-centric approach to therapy allowing for increases in energy and stimulation sessions based on your needs to ensure the best possible outcome.
The procedure is completed in the operational room under anesthesia. The device will be implanted slightly above the ankle area as shown in the image above. The device is permanent and MRI-friendly. The implant does not create any risk or deviation to your daily life.
Eligibility criteria vary depending on the study. Patients may qualify for one or more clinical trials if they meet certain study-specific requirements. For additional study requirements and eligibility information, please contact our Research Department by emailing research@theupi.com or calling 210-617-3670 and selecting the Research option. A member of our team will be happy to answer your questions and discuss available study opportunities.
