Clinical Evidence

The Phagenyx® Neuromodulation System improves swallowing safety and efficiency by restoring the brain’s ability to initiate and coordinate safe swallowing, accelerating recovery from post-stroke dysphagia

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Pioneering Dysphagia Research

Years of groundbreaking research in swallowing neurophysiology and pharyngeal electrical stimulation (PES) have advanced our understanding of dysphagia recovery. This foundational science has redefined how the field approaches treatment, opening new pathways for restoring safe and efficient swallowing.

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Mechanistic studies, validated by fMRI and MEG

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Randomized controlled trials

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Peer-reviewed publications

See How Phagenyx Delivers:

Phagenyx Accelerates Return to Oral Nutrition

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Suntrup-Krueger et al. (Crit Care 2023) report that pharyngeal electrical stimulation led to a 6-day faster return to full oral nutrition (4.3 vs 10.2 days) and halved the rate of feeding-tube dependency at discharge (27 % vs 53 %) in post-extubation stroke patients.

1. Suntrup-Krueger et al. Crit Care. 2023;27(1):383

Phagenyx Reduces Aspiration Risk

Pharyngeal electrical stimulation improves swallowing safety, with patients demonstrating a two-fold reduction in aspiration risk and significant decreases in dysphagia severity scores (FEDSS). These outcomes support safer oral intake and reduced reliance on feeding tubes.

1. Suntrup-Krueger et al. Neurotherapeutics. 20252. Dziewas R et al. Lancet Neurol. 2018;17(10):849-859.

Phagenyx Shortens Total Length of Stay

Across recent multicenter studies, pharyngeal electrical stimulation (PES) shortened hospital and ICU length of stay and increased rates of early tracheostomy decannulation. Patients treated with PES achieved faster recovery, supporting earlier discharge readiness.

1. Suntrup-Krueger et al. Neurotherapeutics. 20252. Dziewas R et al. Lancet Neurol. 2018;17(10):849-859.

Phagenyx Restores Swallowing Function in Patients Unresponsive to Standard of Care 

After 7 weeks of no progress, patients treated with Phagenyx showed measurable return to oral intake within 3 days – reaching 76% at 90 days.

Standard of care (mean 7 weeks): Days 10, 20, 30, 50; n=150. .Post PES treatment: Within 3 Days; n=145, Within 14 Days: n=141, Within 90 Days: n=124.

1. Internal analysis of PHADER data subset. Unpublished data provided to FDA for review as part of DEN220025.

Key Publications

PES linked to positive swallow and diet intake outcomes including DSRS, PAS and FOIS scores

PES linked to increase in swallow-related neurotransmitter Substance P

After PES treatment, 75% of patients improved swallowing function and were able to be decannulated

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