RecruitingNot ApplicableNCT07780981

Impact of Body Positioning on EndoFLIP Measurements: A Comparative Study of Supine and Left Lateral Decubitus Positions


Sponsor

Johns Hopkins University

Enrollment

25 participants

Start Date

Jul 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective, single-center, crossover study comparing EndoFLIP measurements obtained in two patient positions, supine and left lateral decubitus, in pediatric and young adult patients. The Endoluminal Functional Lumen Imaging Probe (EndoFLIP) is an FDA-approved device for patients aged 5 and older that utilizes high-resolution impedance planimetry and volume-controlled distension to assess esophagogastric junction function. Currently, no standardized positioning protocol exists, and proceduralists perform EndoFLIP based on individual preference, either supine or left lateral decubitus. This variability may introduce measurement inconsistencies, particularly when comparing preoperative and postoperative assessments performed in different positions.


Eligibility

Min Age: 5 YearsMax Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying EndoFlip for people with dysphagia, eosinophilic esophagitis (eoe), and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 5 Years to 21 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTEndoFlip

The Endoluminal Functional Lumen Imaging Probe (EndoFLIP) is an FDA-approved device for patients aged 5 years and older and it utilizes high-resolution impedance planimetry and volume-controlled distension to evaluate the GI lumen.


Locations(1)

Charlotte R. Bloomberg Children's Center

Baltimore, Maryland, United States

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NCT07780981


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