Can a stomach stent predict who gets better? small study tests new approach for gastroparesis
NCT ID NCT04287647
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether placing a temporary metal stent in the stomach outlet could predict if a patient with severe gastroparesis would later benefit from a permanent procedure called GPOEM. Only 8 adults with gastroparesis that didn't improve with standard treatments took part. The study was terminated early, so results are limited.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
transpyloric stent (a temporary metal stent placed in the stomach outlet)
What this could lead to
If successful, this could help doctors identify which patients with severe gastroparesis will benefit from a permanent procedure called GPOEM.
What could go wrong
This is a very small, early study (only 8 people) that was terminated early. The stent is temporary and only used as a test, not a treatment itself.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for GASTROPARESIS are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Northwestern University
Chicago, Illinois, 60611, United States