Status:
COMPLETED
Evaluation of Lotrafilcon A Lenses Over a Three Month Period
Lead Sponsor:
CIBA VISION
Conditions:
Myopia
Eligibility:
All Genders
Phase:
NA
Brief Summary
The purpose of this trial is to assess the performance of a Lotrafilcon A contact lens over a 3-month period.
Eligibility Criteria
Inclusion
- On examination, have ocular findings considered to be "normal" and which would not prevent a subject from safely wearing contact lenses.
- Be willing and able to follow instructions and meet the schedule of follow-up visits as defined in the informed consent.
- Be able to wear the study lenses in the available powers.
- Currently wear contact lenses for a minimum of 5 days a week, and at least 8 hours a day.
- Other protocol inclusion/exclusion criteria may apply.
Exclusion
- Eye injury or surgery within twelve weeks immediately prior to enrollment for this trial.
- Pre-existing ocular irritation that would preclude contact lens fitting.
- Currently enrolled in an ophthalmic clinical trial.
- Evidence of systemic or ocular abnormality, infection or disease likely to affect successful wear of contact lenses or use of their accessory solutions.
- Any use of medications for which contact lens wear would be contraindicated, in the opinion of the investigator.
- History of corneal refractive surgery.
- Other protocol inclusion/exclusion criteria may apply.
Key Trial Info
Start Date :
May 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2009
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT00931307
Start Date
May 1 2009
End Date
September 1 2009
Last Update
June 29 2012
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