New device could speed up GERD diagnosis and save billions

NCT ID NCT07227506

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a new FDA-approved device called MuVI that measures electrical resistance in the esophagus to diagnose GERD and eosinophilic esophagitis. Researchers will enroll 50 adults with chronic esophageal symptoms who are already scheduled for an upper endoscopy. The goal is to see if this device can diagnose these conditions more accurately and cost-effectively than current methods, potentially reducing the need for multiple procedures.

What this could mean

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

Active substance

MuVI Esophageal mucosal impedance testing device

What this could lead to

If successful, this device could provide a faster, cheaper, and more accurate way to diagnose GERD and eosinophilic esophagitis, reducing the need for multiple procedures.

What could go wrong

This is a small early study with only 50 participants, so results may not apply to everyone. The device may not be more accurate than current tests.

Disclaimer Read more

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.

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Conditions

The condition(s) this trial relates to.

eosinophilic esophagitis gastroesophageal reflux disease

As listed by the trial registrant

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

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Froedtert Hospital

    RECRUITING

    Milwaukee, Wisconsin, 53226, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••