Phagenyx® Registry Study

Recruiting now

Conditions studied: Dysphagia

In brief

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).

Key facts

Study ID

NCT06866418

Run by

Phagenesis Ltd.

People needed

600

Starts

2025-09-15

Expected to finish

2036-09-01

Last updated by the study team

2026-07-09

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Phagenyx® System Group Patients: Patients underwent treatment with the Phagenyx® System for a minimum of 3 treatments.
• Control Group Patients: Patient requires a nasogastric feeding tube for severe dysphagia and required dysphagia treatment.
• Willing and able to provide appropriate informed consent (if required).

You may not qualify if…

• Primary endpoint outcome data not collected or not available.
• In the investigator or sponsor's opinion the patient is not considered suitable.
• Participation in another interventional study (medicinal or device) that could influence the outcomes of PES.
• Treatment of dysphagia with other forms of electrical stimulation.

Where it is running

• Banner University Medical Center — Phoenix, Arizona, United States (enrolling)
• HMH Jersey Shore University Medical Center — Neptune City, New Jersey, United States (enrolling)
• University of Texas — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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