Study: Manometry With & Without Lidocaine

Completed · Not applicable

Conditions studied: Normal

In brief

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 as compared to HRPM conducted without anesthetic.

Key facts

Study ID

NCT03349112

Run by

University of Wisconsin, Madison

People needed

36

Starts

2015-12-22

Expected to finish

2018-11-09

Last updated by the study team

2019-10-02

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male and female adults 18-65.
• All races.
• Able to consent for self.

You may not qualify if…

• 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

Where it is running

• University of Wisconsin - Madison — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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