N/A
Completed N=20
Treatment of Dysphagia by Using a Synchronized Electrical Stimulation Device
Deglutition Disorders
Source: ClinicalTrials.gov NCT02718963 ↗
Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Nov 2020
Primary outcomePrimary: Pressure and Timing Change of Velopharynx, Tongue Base, Low Pharynx and Upper Esophageal Sphincter. — 162.04; 129.66; 200.90; 170.66 mmHg — p=< 0.05
Summary
The purpose of this study is to determine the synchronized electrical stimulation device effective in the treatment of dysphagia.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pressure and Timing Change of Velopharynx, Tongue Base, Low Pharynx and Upper Esophageal Sphincter. |
162.04; 129.66; 200.90; 170.66; 81.59; 136.40 | < 0.05 sig |
Eligibility Criteria
Inclusion Criteria
- who have dysphagia symptoms and verified deglutition disorder by video fluoro swallowing study
Exclusion Criteria
- who reject the checkup their deglutition function by high resolution manometry
- who reject apply "Synchronized Electrical Stimulator"
Data sourced from ClinicalTrials.gov (NCT02718963). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.