Gastric Electrical Stimulation for Abdominal Pain in Gastroparesis

Status Terminated

Clinical Trial Summary

To conduct a pilot study to evaluate the effects of new GES programming settings on abdominal pain in patients with gastroparesis and existing GES devices, whose abdominal pain has so far been refractory to drugs and/or devices.

Clinical Trial Description

Eligible patients will undergo detailed pain assessments as well as non-invasive physiologic assessment. Patients existing GES devices will be reprogrammed to new setting for 4 week and their GI symptoms including pain will be evaluated by a daily diary. At the end of 4 weeks detailed pain assessments and noninvasive physiologic assessments will be repeated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04121325
Study type	Observational
Source	University of Louisville
Contact
Status	Terminated
Phase
Start date	December 18, 2019
Completion date	March 13, 2020

View Details

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