Status:
COMPLETED
Comparison of Two Marketed Lenses in a Controlled Environment
Lead Sponsor:
Johnson & Johnson Vision Care, Inc.
Conditions:
Eye Dryness
Eligibility:
All Genders
18-50 years
Phase:
NA
Brief Summary
This study is comparing two silicone hydrogel contact lenses in a controlled environment for identification of characteristics associated to vision.
Eligibility Criteria
Inclusion
- The subject must be 18 years of age and less than 51 years of age;
- The subject must have read and understood the Participant Information Sheet;
- The subject must have read, signed and dated the Informed Consent;
- The subject must be a current planned replacement soft contact lens wearer;
- The subject must be a regular user of devices (computer, tablet and/or smart phone) for a minimum average of 5 ± 1 hours per day in a typical week
- The subject must have a refractive error within the range of correction of both study contact lenses;
- The subject must have a best-corrected visual acuity of 6/9 (20/30, 0.18 LogMAR) or better in each eye;
- The subject must demonstrate an acceptable fit with both study contact lenses;
- The subject must agree to wear their contact lenses as directed for the duration of the study (every day or for at least a minimum of five days per week for a minimum of six hours per day and be willing and able to adhere to the instructions set in the clinical protocol and maintain the appointment schedule;
- The subject must have normal eyes with the exception of the need for visual correction.
Exclusion
- Any known sensitivity or intolerance to any of the contact lenses or adjunct products to be used.
- Monocular vision (only one eye with functional vision or only one eye fitted with contact lenses).
- Use of systemic or ocular concomitant medications which, as determined by the investigator, might contraindicate or interfere with contact lens wear.
- Ocular anterior segment infection, inflammation, abnormality, or active disease, which would contraindicate contact lens wear.
- Any moderate or severe ocular condition observed during slit lamp examination at the enrollment visit.
- A history of herpetic keratitis, ocular surgery or irregular cornea(s).
- Known pregnancy or lactation during the study period.
- Enrollment of investigator's office staff, relatives, or members of their respective households.
- Participation in any clinical trial within 30 days of the enrollment visit.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2014
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT02212301
Start Date
July 1 2014
End Date
December 1 2014
Last Update
October 28 2016
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
London, United Kingdom, SW1E 6AU