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CompletedNCT00638846

Performance of Two Silicone Hydrogel Toric Contact Lenses

Multi-Center Evaluation Of Two Silicone Hydrogel Toric Contact Lenses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
276 (actual)
Sponsor
Johnson & Johnson Vision Care, Inc. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Evaluation of the clinical performance of two toric contact lenses in a 2-week, single masked (subject), daily wear, randomized, bilateral, parallel group study.

Conditions

Interventions

TypeNameDescription
DEVICEsenofilcon A toricsilicone hydrogel toric lens, worn daily for 2 wks (2wks replacement)
DEVICEbalafilcon A toricsilicone hydrogel toric lens, worn daily for 2 wks (2wks replacement)

Timeline

Start date
2008-02-01
Primary completion
2008-05-01
Completion
2008-05-01
First posted
2008-03-19
Last updated
2015-05-21
Results posted
2010-07-19

Locations

19 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00638846. Inclusion in this directory is not an endorsement.

Performance of Two Silicone Hydrogel Toric Contact Lenses (NCT00638846) · Clinical Trials Directory