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A Study to Evaluate the Safety and Effectiveness of Oculeve Intranasal Lacrimal Neurostimulator in Participants With Dry Eye Syndrome

Dry Eye Syndrome Clinical Trial

Official title:
A Randomized, Controlled, Double-Masked, Multicenter Trial Designed to Evaluate Acute Tear Production With the Oculeve Intranasal Lacrimal Stimulator Compared to Two Control Applications in Patients With Aqueous Deficient Dry Eye

Clinical Trial Summary

The purpose of this study is to compare acute tear production produced by the Oculeve Intranasal Lacrimal Neurostimulator with two control devices in participants with aqueous tear deficiency.

Clinical Trial Description

This is a prospective, randomized, controlled, double-masked, multicenter clinical trial in which participants with aqueous tear deficiency will receive three different device applications in a randomized sequence. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02680158
Study type Interventional
Source Oculeve, Inc.
Contact
Status Completed
Phase N/A
Start date January 31, 2016
Completion date March 31, 2016
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