Comparative Assessment of Lipid Layer Thickness Measurements
ConditionDry Eye
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorIndiana University
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Dry eye disease
Disqualifiers
None
Trial population
Patients presenting to the clinic with dry eye disease symptoms will be included in the study.
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
LipiView
DeviceSubjects will undergo lipid layer thickness measurement
Omnicad
DeviceSubjects will undergo lipid layer thickness measurement
Bruder Ocular Surface Analyzer
DeviceSubjects will undergo lipid layer thickness measurement
Treatment groups
50 Participants
are divided into 1 treatment groupGroup A: Dry Eye3 interventions
Trial outcomes
Primary outcomes
1
Lipid Layer Thickness
Average and minimum lipid layer thickness measurements will be compared across devices
Time frame
measurements taken at single visit, baselineSecondary outcomes
1
Correlation with dry eye clinical measurements
Correlations will be compared and analyzed with clinical dry eye measuremetns
Time frame
measurements taken at single visit, baselineSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov