Actively Recruiting

Age: 18Years - 100Years
All Genders
ID07579130

Comparative Assessment of Lipid Layer Thickness Measurements Across Three Devices and Their Correlation With Clinical Indicators in Dry Eye Disease

Led by Indiana University · Updated on 2026-05-11

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the measurements of ocular lipid layer thickness (LLT) taken by three commonly used clinical devices to compare their agreement and consistency. The study also aims to find which device's LLT measurements best correlate with established clinical indicators of dry eye disease severity. Participants with dry eye disease will have their lipid layer thickness measured using three different devices: LipiView, Omnicad, and Bruder Ocular Surface Analyzer. These measurements will be taken during a single visit in a random order to ensure unbiased comparison. During the study visit, participants will undergo LLT measurement with all three devices. Researchers will analyze the measurements and compare them to clinical assessments of dry eye severity. The main outcome is the LLT measurement at baseline, alongside the correlation with clinical dry eye indicators. The study participation involves a single visit and does not include any treatment or long-term follow-up.

CONDITIONS

Brief Title

Comparative Assessment of Lipid Layer Thickness Measurements

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Dry eye disease
  • Age between 18 and 100 years
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - 1 day

Participants with dry eye disease undergo lipid layer thickness measurements using three different devices in random order during a single visit.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Atwater Eye Care Center

Bloomington, Indiana, United States, 47405

Actively Recruiting

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Research Team

A

Anna Tichenor

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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