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In this study the investigators plan to enroll three groups of patients: non-Sjogren's dry eye, Sjogren's dry eye and controls. The study has the following primary goals:
Enrollment
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Volunteers
Inclusion criteria
Male or female aged 18 or older
Capacity to give informed consent
Self-reported literacy
Best corrected visual acuity at distance 20/40 in each eye
Signed Institutional Review Board (IRB)-approved consent agreeing to the terms of the study For Sjogren's-related dry eye, the below inclusion criteria will be required
Exclusion criteria
● Age less than 18 years
13 participants in 3 patient groups
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Central trial contact
Richard C Medina, BA
Data sourced from clinicaltrials.gov
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