Status:
COMPLETED
Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses (Study 2)
Lead Sponsor:
Alcon Research
Conditions:
Refractive Error
Eligibility:
All Genders
18-45 years
Phase:
NA
Brief Summary
The purpose of this study is to compare the subjective performance of two daily disposable contact lenses with respect to comfort and handling.
Eligibility Criteria
Inclusion
- Adapted soft contact lens wearer;
- Spherical distance contact lens prescription between -1.00 and -6.00 diopter (inclusive);
- Spectacle cylinder ≤0.75 diopter in the least astigmatic eye, ≤1.00 diopter in the other;
- Correctable to 6/9 (20/30) in both eyes;
- Read, understand, and sign the informed consent;
- Willing to comply with the wear schedule;
- Willing to comply with the study visit schedule;
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Any active corneal infection, injury or inflammation;
- Systemic or ocular allergies which might interfere with contact lens wear;
- Systemic or ocular disease which might interfere with contact lens wear;
- Strabismus or amblyopia;
- Corneal refractive surgery and any anterior segment surgery;
- Use of systemic/topical medication contraindicating contact lens wear;
- Use of gas permeable contact lenses within 1 month preceding the study;
- Participation in any concurrent clinical trial or in the last 30 days;
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
September 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2013
Estimated Enrollment :
86 Patients enrolled
Trial Details
Trial ID
NCT01917162
Start Date
September 1 2013
End Date
November 1 2013
Last Update
November 7 2013
Active Locations (1)
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1
Visioncare Research Ltd
Farnham, Surrey, United Kingdom, GU9 7EN