Tracking a promising therapy for stomach paralysis

NCT ID NCT05047289

ENROLLING_BY_INVITATION Knowledge-focused Sponsor: Indiana University Source: ClinicalTrials.gov ↗

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study creates a registry of people with gastroparesis—a condition where the stomach empties too slowly, causing nausea, vomiting, and pain—who have received a gastric electrical stimulation (GES) device. The goal is to collect long-term data to help researchers understand how GES works and to support the development of better treatments. Participants are those who have already had the device implanted for their symptoms.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance: gastric electrical stimulation device
What this could lead to: If successful, this registry could provide valuable data to improve treatments and diagnostics for gastroparesis.
What could go wrong: This is an observational registry, not a treatment trial, so it will not directly test whether GES works. Results depend on the quality and completeness of the data collected.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

gastroparesis Nausea Vomiting

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

GASTROPARESIS

Contacts and locations

Locations

Indiana University Hospital

Indianapolis, Indiana, 46202, United States

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