Pilot Study to Clinical Evaluate Device Prototypes in Dry Eye Patients

NCT01957670 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2016-03-08

No results posted yet for this study

Summary

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

Conditions

  • Dry Eye Syndrome

Interventions

DEVICE

Lacrima medical Prototypes

Sponsors & Collaborators

  • Lacrima Medical LTD

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2016-04-30
Completion
2016-04-30

Countries

  • Israel

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01957670 on ClinicalTrials.gov