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NCT00584623 Clinical Trial

Simultaneous Fluoroscopic and Endoscopic Examination of the Oropharyngeal Phase of Deglutition

Dysphagia Clinical Trial

Official title:
Simultaneous Fluoroscopic and Endoscopic Examination of the Oropharyngeal Phase of Deglutition

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00584623
Other study ID # 200715188
Secondary ID
Status Withdrawn
Phase N/A
First received December 26, 2007
Last updated May 26, 2017
Start date March 2007
Est. completion date June 2008

Study information
Verified date May 2017
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To correlate findings between two commonly-used types of swallowing studies: videofluoroscopy and flexible endoscopic evaluation of swallowing (FEES).

Description:

The specific aim of this study is to correlate findings between two commonly-used types of swallowing studies: videofluoroscopy and flexible endoscopic evaluation of swallowing (FEES). Specifically, the timing of swallowing events will be correlated between teh two studies. In addition, the pharyngeal constriction ratio (a validated measure of pharyngeal strength on videofluoroscopy) will be compared with the pharyngeal squeeze maneuver (an assessment of pharyngeal strength on FEES), with the hypothesis that there will be a strong correlation between PCR and pharyngeal squeeze.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- complaints of dysphagia

- scheduled to undergo videofluoroscopy

- able to tolerate both videofluoroscopic evaluation of swallowing and FEES

Exclusion Criteria:

- age less than 18

- contraindications to videofluoroscopy (reaction to barium, possible pregnancy)

- contraindications to FEES (bilateral obstructing nasal pathology or nasopharyngeal stenosis)

- specific/vulnerable populations (children, mentally handicapped, pregnant women, fetuses, prisoners, cognitive impairment, life-threatening disease, social or economic disadvantage)

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of California Davis Medical Center Sacramento California

Sponsors (1)
Lead Sponsor Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

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