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Predicting the Success of Dry Eye Disease Interventions Using Clinical Tests — PreDICT  

Dry Eye Clinical Trial

Official title:
Predicting the Success of Dry Eye Disease Interventions Using Clinical Tests

Clinical Trial Summary

This is a single site, prospective, cross-sectional, controlled clinical study on a total of 66 subjects. The subjects are divided into two groups: Hypertonic Saline Non-Responders (33 subjects) and Hypertonic Saline Responders (33 subjects). After completion of questionnaires, the subjects will undergo Dry Eye Disease testing and functional nerve testing. Subjects who qualify will be dispensed 4 weeks of preservative free artificial tears and instructed to instill one drop into each eye twice daily. Subjects will return for a follow up visit 4 weeks later (± 4 days), during which subjects will complete the questionnaires again and the Dry Eye Disease tests and functional nerve tests will be repeated.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04125134
Study type Interventional
Source Tufts Medical Center
Contact Nancy Gee, MPH
Phone 617-636-5489
Email ngee@tuftsmedicalcenter.org
Status Recruiting
Phase Phase 4
Start date October 3, 2019
Completion date December 2024
View Details
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