HydroCision is committed to proving the clinical efficacy of its products through postmarket, controlled, IRB-approved clinical studies.
The following study is currently enrolling patients in the United States.
The TenJet Patient Registry
The TenJet Patient Registry research project will help us systematically gather and analyze data to understand how effective TenJet is in treating chronic tendinopathy in the elbow, hip, and shoulder.
Past Clinical Studies
TenJet Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) was a prospective, multicenter, single-arm, observational study to evaluate clinical outcomes for patients presenting with chronic lateral or medial epicondylitis and choosing a percutaneous tenotomy treatment using the HydroCision TenJet device.