Status:
COMPLETED
Study: Manometry With & Without Lidocaine
Lead Sponsor:
University of Wisconsin, Madison
Conditions:
Normal
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The purpose of this study is to determine whether subjects report a difference in comfort with High Resolution Pharyngeal Manometry (HRPM) conducted following application of lidocaine as an anesthetic...
Detailed Description
High resolution pharyngeal manometry (HRPM) is used for assessing swallowing pressure along the length of the pharynx and upper esophageal sphincter. Pressure measurements in the region of the velopha...
Eligibility Criteria
Inclusion
- Healthy male and female adults 18-65.
- All races.
- Able to consent for self.
Exclusion
- History of dysphagia.
- History of previous pharyngeal or esophageal manometry.
- History of facial fracture or abnormalities precluding passage of catheter through nares.
- History of esophageal pathology including previous resection or perforation.
- Pregnant
- Known lidocaine allergy or sensitivity
Key Trial Info
Start Date :
December 22 2015
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 9 2018
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT03349112
Start Date
December 22 2015
End Date
November 9 2018
Last Update
October 2 2019
Active Locations (1)
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1
University of Wisconsin - Madison
Madison, Wisconsin, United States, 53792