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Pilot Study to Clinical Evaluate Device Prototypes in Dry Eye Patients

Dry Eye Syndrome Clinical Trial

Official title:
Pilot, Open-label, Single-Arm Study Designed to Clinically Evaluate Various Lacrima Medical Device Prototypes in Adult Patients With Dry Eye Syndrome

Clinical Trial Summary

The study will assess the safety, tolerability and feasibility of Lacrima investigational medical device to treat dry eye patients

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01957670
Study type Interventional
Source Lacrima Medical LTD
Contact
Status Withdrawn
Phase N/A
Start date February 2014
Completion date April 2016
View Details
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