Safety and Efficacy Assessment of Vismed® (Sodium Hyaluronate) for the Treatment of Dry Eye Syndrome
This study has been completed.
Sponsor:
Lantibio
Collaborators:
River Plate Biotechnology, Inc.
Rx Development Resources, LLC
Information provided by:
Lantibio
ClinicalTrials.gov Identifier:
NCT00599716
First received: January 11, 2008
Last updated: January 8, 2009
Last verified: January 2009
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study has been completed. |
|---|---|
| Study Completion Date: | May 2008 |
| Primary Completion Date: | April 2008 (Final data collection date for primary outcome measure) |