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Trials / Terminated

TerminatedNCT04143841

Viveye Ocular Magnetic Neurostimulation System (OMNS) for the Management of Severe Dry Eye Disease

A Pilot Study to Evaluate the Safety and Effectiveness of the Viveye Ocular Magnetic Neurostimulation System (OMNS) for the Management of Severe Dry Eye Disease

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Epitech Mag Ltd. · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the safety and effectiveness of Viveye OMNS non-invasive treatment for management of the signs and symptoms of severe dry eye disease.

Conditions

Interventions

TypeNameDescription
DEVICEViveye OMNS treatmentThe Viveye OMNS treatment ( \~30 min) will be applied once, during the treatment visit only
DEVICEViveye OMNS sham treatmentThe Viveye OMNS sham treatment ( \~30 min) will be applied once, during the treatment visit only

Timeline

Start date
2019-10-30
Primary completion
2021-01-06
Completion
2021-01-06
First posted
2019-10-29
Last updated
2021-04-21

Locations

3 sites across 1 country: Israel

Source: ClinicalTrials.gov record NCT04143841. Inclusion in this directory is not an endorsement.

Viveye Ocular Magnetic Neurostimulation System (OMNS) for the Management of Severe Dry Eye Disease (NCT04143841) · Clinical Trials Directory