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Sponsors and Collaborators: |
University of Melbourne Clinical Vision Research Australia Cooper Companies |
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Information provided by: | University of Melbourne |
ClinicalTrials.gov Identifier: | NCT00346593 |
The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.
Condition | Intervention |
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Myopia |
Device: Silicone hydrogel contact lens |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Single Group Assignment |
Ages Eligible for Study: | 18 Years to 45 Years |
Genders Eligible for Study: | Both |
Inclusion Criteria:
Exclusion Criteria:
Australia, Victoria | |
Clinical Vision Research Australia | |
Carlton, Victoria, Australia, 3053 |
Principal Investigator: | Carol Lakkis, BScOptom PhD | Clinical Vision Research Australia |
Study ID Numbers: | H03 010 |
Study First Received: | June 29, 2006 |
Last Updated: | February 8, 2007 |
ClinicalTrials.gov Identifier: | NCT00346593 |
Health Authority: | Australia: Department of Health and Ageing Therapeutic Goods Administration |
Myopia |