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Gastric Electrical Stimulation for Abdominal Pain in Gastroparesis

NCT04121325 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 4

Last updated 2023-10-27

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Enterra

To measure validated and subjective pain scores among patients with an existing GES device, and who have a trial of new settings directed at abdominal pain and compare their pain scores to each patient baseline symptoms, done with their previous GES settings.

Sponsors & Collaborators

  • University of Louisville

    lead OTHER

Principal Investigators

  • Thomas Abell, MD · University of Louisville

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-18
Primary Completion
2020-03-13
Completion
2020-03-13
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04121325 on ClinicalTrials.gov