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Study identifier: NCT05180253 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Esophageal and Gastric Registry and Biorepository

Condition: Gastro Esophageal Reflux  ·  Sponsor: University of Louisville

PhaseN/A
Planned participants40
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersYes

About this study

The evaluation of the foregut, the esophagus and stomach, has come a long way over the past two decades, and continues to experience exciting discoveries in the clinical evaluation of foregut physiology. Assessing esophageal peristalsis has relied for the past several decades on High Resolution Manometry (HRM), however it has recently become known that even though HRM is an extremely effective tool, that there are certain subsets of patients in which additional information is required. Additionally, the assessment of esophageal reflux disease has relied on pH impedance for the last two decades. However, this procedure requires a catheter to be passed through a nostril and remain in place for at least 24 hours. Novel techniques, already FDA approved, including EndoFLIP for esophageal peristalsis and mucosal integrity (MI) for reflux disease, have emerged as time-of-endoscopy assessments. Both involve the placement of a balloon through the scope at time of upper endoscopy (standard first line assessment for both dysphagia and reflux symptoms) and are quick and pose little-to-no additional risk or discomfort for patients. However, data regarding normal esophageal parameters are poorly defined for both EndoFLIP and MI. Additionally, EndoFLIP has increasingly been used to assess the pylorus, and scarce data exists there regarding how a tool originally envisioned for esophageal assessment can be used more distally in the GI tract. We will recruit healthy, asymptomatic volunteers t…

This description comes directly from the study's public registry record.

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Locations (1)

Norton HealthcareLouisville, Kentucky, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05180253