N/A N=20 Randomized Treatment

Treatment of Dysphagia by Using a Synchronized Electrical Stimulation Device

Deglutition Disorders

Bottom Line

View on ClinicalTrials.gov: NCT02718963 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Nov 2020

Primary outcome: Primary: 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

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Synchronized Electrical Stimulation Device (Device)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Seoul National University Hospital
Primary completion: Jun 2016

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

Summary

The purpose of this study is to determine the synchronized electrical stimulation device effective in the treatment of dysphagia.

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"

View full record on ClinicalTrials.gov →

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.