Pilot Study to Clinical Evaluate Device Prototypes in Dry Eye Patients
NCT01957670 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2016-03-08
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
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