Phase
Condition
Presbyopia
Treatment
Deleficon A (multifocal)
Senofilcon A (multifocal)
Clinical Study ID
Ages > 42 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Are at least 42 years of age and has full legal capacity to volunteer;
Have signed an information consent letter;
Are willing and able to follow instructions and maintain the appointment schedule;
Habitually wears soft contact lenses for the past 3 months (minimum);
Are presbyopic and require a reading addition of at least +0.75D and no more than +1.75D;
Can be refracted and achieve monocular spectacle distance vision of at least 20/25Snellen (or +0.10logMAR) visual acuity;
Have contact lens power requirements that fall within the available study lensparameters (distance sphere: +6D to -9D; near addition as per each lens design);
Can be fit with the initial fitting guidelines provided by the lens manufacturer anduse either Low or Medium Add (same add in both eyes).
Exclusion
Exclusion Criteria:
Are a current habitual wearer of Dailies Total1 Multifocal or ACUVUE OASYS MAX 1-DAYMultifocal;
Has refractive astigmatism higher than -0.75DC in either eye;
Are participating in any concurrent clinical or research study involvingintervention or invasive ocular tests;
Have any known active ocular disease and/or infection;
Has a systemic condition that in the opinion of the investigator may affect a studyoutcome variable;
Are using any systemic or topical medications that in the opinion of theinvestigator may affect a study outcome variable;
Have known sensitivity to the diagnostic pharmaceuticals to be used in the study;
Have undergone refractive error surgery;
Are a member of the Centre for Ocular Research & Education (CORE) directly involvedin the study.
Study Design
Connect with a study center
Centre for Ocular Research & Education (CORE)
Waterloo, Ontario N2L 3G1
CanadaSite Not Available
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