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A Prospective, Multicenter, Open-label, Safety and Preliminary Efficacy Study of the Surgical Implantation of OPKO's Glaucoma Drainage Device (AquashuntTM) in Patients With Refractory Chronic Forms of Open Angle Glaucoma (OAG)

This study has been completed.
Sponsor:
Information provided by:
OPKO Health, Inc.
ClinicalTrials.gov Identifier:
NCT00834223
First received: February 2, 2009
Last updated: March 31, 2011
Last verified: March 2011
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: May 2010
  Primary Completion Date: September 2009 (Final data collection date for primary outcome measure)