Clinical Evaluation of Lifitegrast Ophthalmic Solution 5.0% in Dry Eye Disease Using In Vivo Confocal Microscopy

ConditionDry Eye
Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorToyos Clinic

About this trial

This is a single center, open label trial to evaluate Lifitegrast Ophthalmic Solution 5.0% in Dry Eye Disease using In Vivo Confocal Microscopy (IVCM

Eligibility criteria

Qualifiers

1. Subject can read, understand and sign an informed consent letter. 2. Provision of signed and dated informed consent form and HIPAA authorization. 3. Stated willingness to comply with all study procedures and availability for the duration of the study 4. Male or female at least 18 years of age at the time of enrollment 5. Minimum corneal staining of ≥2 or greater according to the NEI grading scale in the lower corneal subregion.

Disqualifiers

1. Have a known hypersensitivity or contraindication to the product or their components.

Trial design

Treatments tested in this trial

  • Lifitegrast Ophthalmic Solution 5.0% (Xiidra)

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators