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Recruiting NCT07579130

Comparative Assessment of Lipid Layer Thickness Measurements

— Observational Dry Eye

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: LipiView, Omnicad, Bruder Ocular Surface Analyzer.
Who it may be relevant to
Registry conditions: Dry Eye. Basic parameters: 18 years — 100 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

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

Overview

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.

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

Primary outcome measures

  • Lipid Layer Thickness [Time frame: measurements taken at single visit, baseline]
Secondary outcome measures (1)
  • Correlation with dry eye clinical measurements [Time frame: measurements taken at single visit, baseline]

Eligibility criteria

Inclusion criteria

  • Dry eye disease

Exclusion criteria

  • None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Atwater Eye Care Center — Bloomington

Identifiers

NCT: NCT07579130 · 29789

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗