About this trial
Characterization of subjective discomfort/pain in patients with ocular surface dysfunction in association with clinical and laboratory parameters, for a better understanding of the underlying pathogenic mechanisms.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
adult patients with suspected or diagnosed DED
Disqualifiers
nothing
Trial population
Participants in the study are patients suffering from ocular disconfort who are referred by their doctors for second/third level diagnostic tests at the University Ophthalmology Department. Patients are adults of both sexes, with eventual concomitant systemic and other ocular pathologies, without any limitation that defines exclusion criteria.
Trial design
Cohort
Other
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Discomfort in subjects affected by Dry Eye Disease (DED)
Assessment of discomfort with Ocular Surface Disease Index (OSDI) and Dry Eye Questionaire-5 (DEQ-5)
Pain in subjects affected by Dry Eye Disease (DED)
Assessment of pain with Visual Analogue Scale (VAS) and Numeric Rating Scale (NRS)
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: