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Summary
A retrospective, open-label, matched-control registry study designed to characterize the effectiveness of Pharyngeal Electrical Stimulation (PES) to improve swallowing in patients with severe dysphagia post stroke when delivered using the Phagenyx® System in real-world clinical settings in hospitals in the United States of America (US).
Official title: Phagenyx® Registry Study: Evaluating Swallowing Therapy Outcomes and Recovery in the U.S.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
600
Start Date
2025-09-15
Completion Date
2036-09
Last Updated
2025-12-22
Healthy Volunteers
No
Conditions
Interventions
1. Phagenyx® System Group Patients
Patients who have undergone Pharyngeal Electrical Stimulation (PES) treatment for severe dysphagia using the Phagenyx® System
Locations (2)
HMH Jersey Shore University Medical Center
Neptune City, New Jersey, United States
University of Texas
Houston, Texas, United States