Using a mucosal impedance device to help diagnose chronic esophageal problems
Official title: Diagnostic Utility of Mucosal Impedance Device in Patients With GERD and Chronic Esophageal Disorders:
Run by Medical College of Wisconsin · NCT07227506 · Data updated 2026-11-12
This test tries a mucosal impedance device during upper endoscopy to see if it helps diagnose people with chronic reflux (GERD) or eosinophilic esophagitis.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Medical College of Wisconsin Academic / other |
| Locations | 1 site (Milwaukee, Wisconsin) |
| Status | Recruiting |
| Started | November 20, 2025 |
| Main results expected | July 1, 2028 |
| Study ends | July 1, 2028 |
| Registry record updated | July 27, 2026 |
| Trial ID | NCT07227506 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with chronic typical or atypical reflux symptoms and/or dysphagia who are already scheduled for upper endoscopy and who do not have exclusions such as pregnancy, active esophageal cancer, stricture, or contraindications to the procedure.
✕Probably not a fit
Patients with esophageal strictures, active esophageal cancer, unstable medical conditions, minors, pregnant people, or those on anticoagulation at the time of procedure are not eligible and unlikely to benefit from this testing.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational study that adds MuVI esophageal mucosal impedance measurements to standard upper endoscopy in participants with chronic esophageal symptoms. Measurements from the impedance device will be compared with endoscopic findings, biopsies, and available pH testing to determine diagnostic concordance. Investigators will also examine potential cost implications by considering whether the device could reduce the need for multiple procedures. Exclusion criteria include esophageal stricture, cancer, unstable condition, anticoagulation on the day of procedure, pregnancy, and minors.
Why it matters
Potential benefit: If successful, the device could speed diagnosis and reduce the need for multiple invasive or costly tests.
How similar studies have gone: Prior research on mucosal impedance has shown promising results for distinguishing GERD from eosinophilic esophagitis and detecting mucosal injury, but larger confirmatory and cost-effectiveness studies are still limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1\. Patients with chronic esophageal symptoms such as atypical or typical reflux symptoms and dysphagia, is here for upper endoscopy testing. Exclusion Criteria: 1. Presence of esophageal stricture 2. Unstable patients who cannot undergo this testing. 3. Patients on anticoagulation on the day of procedure. 4. Presence of esophageal cancer. 5. Pregnancy. 6. Minor patients.
Where it's running
-
Froedtert Hospital
Milwaukee, Wisconsin, United States Recruiting
Study contacts
- Study coordinator: Gokulakrishnan Balasubramanian
- Email: gbalasubramanian@mcw.edu
- Phone: 414-805-3827
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.