Clinical Trial

Standardizing Swallow Pressure Measurements

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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.
Protocol Amendment History 2 changes
notable Primary completion pushed: 2027-05 -> 2027-06 2026-05-30
minor Completion pushed: 2027-05 -> 2027-06 2026-05-30
Trial Details
NCT Number NCT07475091
Lead Sponsor University of Wisconsin, Madison
Conditions Dysphagia
Enrollment 25 participants
Start Date 2026-08
Primary Completion 2027-06 (estimated)
Study Completion 2027-06 (estimated)
Updated on ClinicalTrials.gov 2026-07-30