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Comparative Assessment of Lipid Layer Thickness Measurements

NCT07579130 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2026-05-11

No results posted yet for this study

Summary

This study compares ocular lipid layer thickness (LLT) measurements obtained from three commonly used clinical diagnostic devices to evaluate their agreement and consistency. It further examines which device's LLT measurements show the strongest correlation with established clinical indicators of dry eye disease severity.

Conditions

  • Dry Eye

Interventions

DEVICE

LipiView

Subjects will undergo lipid layer thickness measurement

DEVICE

Omnicad

Subjects will undergo lipid layer thickness measurement

DEVICE

Bruder Ocular Surface Analyzer

Subjects will undergo lipid layer thickness measurement

Sponsors & Collaborators

  • Indiana University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-01
Primary Completion
2028-12-20
Completion
2028-12-20
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07579130 on ClinicalTrials.gov