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Bedside Screening Method for Patients With Potential Swallowing Impairment — CABS  

Dysphagia Clinical Trial

Official title:
Development and Validation of Clinician-administered Bedside Screening Method for Patients With Potential Swallowing Impairment

Clinical Trial Summary

Previous studies have shown that most patients with functional oropharyngeal dysphagia could be quickly, safely and accurately recognized by using a clinical bedside method developed by the investigative team as the volume-viscosity swallow test (V-VST) that systematically evaluates the main clinical signs and symptoms of safety and efficacy of swallowing and monitors pulse oximetry to improve the detection of patients with silent aspirations.The aim of this study is to validate this test for persons suspected of having swallowing impairment, using a new thickener, with respect to the Videofluoroscopy (VFS) method (treated as the gold standard).

Clinical Trial Description

n/a

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01158313
Study type Observational
Source Nestlé
Contact
Status Completed
Phase N/A
Start date July 2010
Completion date August 2011
View Details
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