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NCT07475091
Standardizing Swallow Pressure Measurements
Conditions: Dysphagia
Sex: All
Ages: 18 Years – 99 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 25
Sponsor: University of Wisconsin, Madison
Location: University of Wisconsin Madison Wisconsin
Summary
This study aims to directly compare and contrast swallowing pressure and impedance measurements obtained from two high-resolution manometry (HRM) systems: the Laborie LMT Pharyngeal System and the Medtronic ManoScan ESO HRM System in healthy adult volunteers. The primary objective is to determine how differences in catheter diameter, sensor configuration, and acquisition platforms influence measurement outcomes. Twenty-five healthy adults will participate in a single, approximately 2-hour visit; the study will be open for one year for data collection and two years for data analysis.
Eligibility Criteria
Inclusion Criteria:
* without known swallowing disorders
Exclusion Criteria:
* Known swallowing disorder
* Allergy to topical anesthetic
* Allergy to food relevant to study participation (e.g. lactose intolerance)
* Inability to follow direction or remain calm during the experiment.
Source: ClinicalTrials.gov (NCT07475091). StuddyBuddy aggregates publicly available trial information.