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Clinical Trial Summary

The objective of this study is to determine if Gastric Electrical Stimulation may influence vagal outflow via vagal afferent fibers that terminate in the Central Nervous System.


Clinical Trial Description

This study will evaluate male and female patients at least 18 years of age, with gastroparesis, who will or have already undergone the implantation of a GES device

The study will be conducted at one center and approximately 200 subjects will be enrolled.

Subjects undergoing the GES implantation will be enrolled before the implantation and may have a baseline visit. The visit procedures will be conducted at the discretion of the investigator dependent on the clinical condition of the patient at that time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02159586
Study type Observational [Patient Registry]
Source Indiana University
Contact
Status Enrolling by invitation
Phase
Start date November 2012
Completion date December 2020

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