BriTer Eyez Moisture Vue On-Demand Moisture Chamber for Dry Eye
Official title: A Clinical Evaluation of the BriTer Eyez Moisture Vue™ On-Demand Disposable Moisture Chamber in Subjects With Mild to Moderate Dry Eye Disease
Run by University of Rochester · NCT07430735 · Data updated 2026-11-12
This study tests whether wearing the BriTer Eyez Moisture Vue on a two-hour period helps people with mild to moderate dry eye feel and see improvements in tear film and related measures.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 35 (estimated) |
| Sponsor | University of Rochester Academic / other |
| Locations | 1 site (Rochester, New York) |
| Status | Recruiting |
| Started | September 1, 2026 |
| Main results expected | July 1, 2027 |
| Study ends | July 1, 2027 |
| Registry record updated | September 11, 2026 |
| Trial ID | NCT07430735 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older with a clinical diagnosis of mild to moderate dry eye who wear eyeglasses.
✕Probably not a fit
Individuals with conditions or factors that could confound results, or those who do not respond to this device, may not experience benefits.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study evaluates the short-term effects of the BriTer Eyez Moisture Vue On-Demand Disposable Moisture Chamber on tear-film stability, tear volume, and tear osmolarity in adults with mild to moderate dry eye disease. Participants will wear the device for two hours, and outcomes related to tear film and symptoms will be assessed. The trial is conducted at the University of Rochester Medical Center with adults who wear eyeglasses and meet the inclusion criteria. Exclusion criteria include pregnancy, cognitive impairment, certain ocular or systemic conditions, and other factors that could confound results. The study aims to provide initial data on whether this device can improve tear-related parameters and symptoms in the short term.
Why it matters
Potential benefit: If successful, participants may experience temporary relief of dry eye symptoms and improvements in tear film quality while using the device.
How similar studies have gone: Prior research on similar moisture-chamber approaches has shown promise for short-term tear-film improvements, though results can vary by device and population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years of age or older * Clinical Diagnosis of mild to moderate dry eye * Individual wears eyeglass spectacles Exclusion Criteria: * Children under the age of 18 years of age * Women who are currently pregnant or nursing * Adults with decisional impairment * Prisoners * Individuals who have a known ocular or medical condition (other than DED) that impacts their ocular surface and could confound the results of the study.
Where it's running
-
University of Rochester Medical Center
Rochester, New York, United States Recruiting
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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.