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:
Opko Health, Inc.
Information provided by:
Opko Health, Inc.
ClinicalTrials.gov Identifier:
NCT00834223
First received: February 2, 2009
Last updated: March 31, 2011
Last verified: March 2011
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
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) |