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[Trial of device that is not approved or cleared by the U.S. FDA]
Sponsored by: Bausch & Lomb, Inc.
Information provided by: Bausch & Lomb, Inc.
ClinicalTrials.gov Identifier: NCT00710879

Responsible Party: Bausch & Lomb, Incorporated ( Mohinder Merchea, OD, PhD )
Study ID Numbers: 568
Study First Received: June 30, 2008
Last Updated: September 19, 2008
ClinicalTrials.gov Identifier: NCT00710879  
Health Authority: United States: Food and Drug Administration

ClinicalTrials.gov processed this record on January 16, 2009