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:
Collaborator:
Pfizer
Information provided by (Responsible Party):
Daniel Moore, University of Kentucky
ClinicalTrials.gov Identifier:
NCT01180062
First received: August 10, 2010
Last updated: December 4, 2014
Last verified: December 2014
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)