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Safety Study of Latanoprost Slow Release Insert (Latanoprost SR)

This study has been terminated.
(Study terminated early due to manufacturer not replenishing study site supply of inserts, despite repeated requests for more inserts.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01180062
First Posted: August 11, 2010
Last Update Posted: December 8, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Pfizer
Information provided by (Responsible Party):
Daniel Moore, University of Kentucky
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been terminated.
  Study Completion Date: June 2014
  Primary Completion Date: June 2014 (Final data collection date for primary outcome measure)