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Sponsors and Collaborators: |
University of Waterloo Ciba Vision, Inc. |
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Information provided by: | University of Waterloo |
ClinicalTrials.gov Identifier: | NCT00371787 |
To evaluate the performance of the study soft lens for vision, comfort, physiology and lens surface properties.
Condition | Intervention | Phase |
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Ametropia |
Device: Soft contact lens |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Official Title: | Evaluation of the Performance of Non-Moulded Soft Contact Lenses |
Enrollment: | 30 |
Study Start Date: | August 2006 |
Study Completion Date: | December 2007 |
Primary Completion Date: | December 2007 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Experimental
Chronic lens wearers
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Device: Soft contact lens
Soft contact lens
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To evaluate the performance of the study soft lens for vision, comfort, physiology and lens surface properties in a group of participants who present with lens related changes.
Ages Eligible for Study: | 17 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Canada, Ontario | |
Centre for Contact Lens Research, University of Waterloo, | |
Waterloo, Ontario, Canada, N2L 3G1 |
Principal Investigator: | Desmond Fonn | Centre for Contact Lens Research |
Responsible Party: | CCLR ( Craig Woods, Research Manager ) |
Study ID Numbers: | P/240/06/CV |
Study First Received: | September 1, 2006 |
Last Updated: | February 13, 2009 |
ClinicalTrials.gov Identifier: | NCT00371787 History of Changes |
Health Authority: | Canada: Health Canada |
Eye Diseases Refractive Errors |
Eye Diseases Refractive Errors |