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Clinical Trial Summary

Evaluation of the effect of Epitomee Device on Gastric Emptying Rate in healthy subjects


Clinical Trial Description

The participants will be enrolled in one investigational site. Subjects meeting eligibility criteria will undergo a gastric emptying test using gastric scintigraphy before any treatment (baseline).

Following the scintigraphy, the subjects will receive Tulip Device treatment - 2 capsules/day.

After repeated capsule intake for either 4 or 11 or 28 days, the subjects will undergo additional gastric emptying test with a capsule intake prior to the test meal. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04485936
Study type Interventional
Source Epitomee medical
Contact
Status Completed
Phase N/A
Start date April 9, 2018
Completion date July 9, 2019

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