A Study to Evaluate Endoflip Normal Ranges Data in Healthy Volunteers

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-03-06

Study Completion Date

2021-06-23

Brief Summary

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The purpose of this research is to establish the normal range of diameter and distensibility of pylorus and the fasting and postprandial antro-pyloric motility in healthy adults.

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Detailed Description

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An Endoflip catheter will be placed through the mouth into the stomach in order to measure distal antral contractile activity and pyloric diameter and distensibility during fasting and after the ingestion of a standard meal

Conditions

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Healthy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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observational study of gastric and pyloric motor function measured with Endoflip

observational study of gastric and pyloric motor function measured with Endoflip during fasting and postprandial periods There is NO intervention

Endoflip measurement of gastric and pyloric function

Intervention Type DIAGNOSTIC_TEST

Endoflip device to measure gastric and pyloric functions

Interventions

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Endoflip measurement of gastric and pyloric function

Endoflip device to measure gastric and pyloric functions

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Females and males.
* Between the ages of 18 and 65 years.
* Body mass index between 18 and 35 kg/m\^2.

Exclusion Criteria

* Heartburn, regurgitation, or symptoms suggestive of gastroparesis such as nausea, early satiety, postprandial bloating, and upper abdominal pain.
* Pregnant

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes