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Clinical Trial Summary

It was well known that aspiration is the primary cause of an aspiration pneumonia among the dysphagia patients.

In order to predict the degree of an aspitation,video-fluoroscopic-swallowing study and fiberoptic-endoscopic swallowing evaluation have been developed, but those evaluations are invasive and allowed only in a limited condition.

In this study, as a precedent study for the non-linear analysis, voice analysis using LPC method will be evaluated. The superiority of LPC method will be compared with a spectral analysis using Jitter and Simmer as a positive control.

This clinical study will be performed prospective, positive-controlled, single-blind (i.e. assessor-blind),and single cohort clinical trial for efficacy


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01981239
Study type Interventional
Source Ulsan University Hospital
Contact
Status Withdrawn
Phase N/A
Start date November 2013
Completion date December 2014

See also
  Status Clinical Trial Phase
Completed NCT00001936 - Electrical Muscle Stimulation to Aid Swallowing in Dysphagia N/A
Completed NCT00001220 - Ultrasound and Videofluoroscopy for Diagnosing Swallowing Disorders N/A
Completed NCT03024333 - Effect of Different Viscous Foods and Liquids on Swallowing Sounds
Completed NCT00013832 - Study of Tongue Pressures N/A
Completed NCT03005093 - The Turkish Feeding/Swallowing Impact Survey N/A
Completed NCT00004566 - Study of Fetal Swallowing N/A
Withdrawn NCT01202968 - Effect of Pre-emptive Transcutaneous Neuro-muscular Electrical Stimulation for Dysphagia in Long Term Intubated Patients N/A