Actively Recruiting
Phagenyx® Registry Study
Led by Phagenesis Ltd. · Updated on 2025-12-22
600
Participants Needed
2
Research Sites
572 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
Phagenyx® Registry Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients treated with the Phagenyx® System for at least 3 treatments
- Patients requiring a nasogastric feeding tube for severe dysphagia and needed dysphagia treatment
- Willing and able to provide appropriate informed consent if required
You will not qualify if you...
- Missing or unavailable primary endpoint outcome data
- Patient considered unsuitable by the investigator or sponsor
- Participation in another interventional study that could affect PES outcomes
- Treatment for dysphagia with other types of electrical stimulation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
HMH Jersey Shore University Medical Center
Neptune City, New Jersey, United States, 07753
Actively Recruiting
2
University of Texas
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
J
Jennifer Miller
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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