A Comparison of 12 Month Daily Wear of Two Novel O2 Permeable Silicone Hydrogel CLs (HOP/SiH) and A Control, Standard O2 Lens

This study has been completed.

Sponsor:

Collaborators:

CIBA VISION

National Eye Institute (NEI)

Information provided by:

University of Texas Southwestern Medical Center

ClinicalTrials.gov Identifier:

NCT00344643

First received: June 23, 2006

Last updated: June 19, 2008

Last verified: June 2008

History of Changes

No Study Results Posted on ClinicalTrials.gov for this Study

About Study Results Reporting on ClinicalTrials.gov

Study Status:	This study has been completed.
Study Completion Date:	December 2006
Primary Completion Date:	December 2006 (Final data collection date for primary outcome measure)

No publications provided by University of Texas Southwestern Medical Center

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Robertson DM, Petroll WM, Cavanagh HD. The effect of nonpreserved care solutions on 12 months of daily and extended silicone hydrogel contact lens wear. Invest Ophthalmol Vis Sci. 2008 Jan;49(1):7-15.

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