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Clinical Trials/NCT00584545
NCT00584545
Withdrawn
Not Applicable

Simultaneous Fluoroscopic and Manometric Measures of the Oropharyngeal Phase of Deglutition

University of California, Davis1 site in 1 countryJune 2007
ConditionsDysphagia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dysphagia
Sponsor
University of California, Davis
Locations
1
Status
Withdrawn
Last Updated
3 years ago

Overview

Brief Summary

To validate the pharyngeal constriction ration, a surrogate measure of pharyngeal strength on fluoroscopy by comparing it with simultaneous pharyngeal manometry.

Detailed Description

The specific aim of this study is to validate the pharyngeal constriction ration, a surrogate measure of pharyngeal strength on fluoroscopy by comparing it with simultaneous pharyngeal manometry. Combined videofluoroscopic swallowing studies with pharyngeal manometry are commonly used in the evaluation of dysphagia. However, no published study has compared the results of simultaneous pharyngeal manometry with objective timing and displacement measures on videofluoroscopy. These objective measures, such as the pharyngeal constriction ratio, were developed here at UCD and are not yet routinely used by other practitioners. A secondary aim of this study will be to corroborate recent data in the literature suggesting that the presence of feeding tube through the upper esophageal sphincter does not affect the oropharyngeal phase of deglutition. This topic is currently under hot debate in the speech language pathology realm and has important implications for the evaluation of hospitalized patients with dysphagia.

Registry
clinicaltrials.gov
Start Date
June 2007
End Date
June 2008
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • undergone pharyngeal manometry with simultaneous videofluoroscopy during the period 1/1/06 to 4/30/07

Exclusion Criteria

  • those who do not meet the inclusion criteria; pregnancy

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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