The effect of Systane Complete and Systane Hydration on subjective comfort, vision and satisfaction with mini-scleral contact lens wear in experienced contact lens wearers

SW Sydney0 个研究点目标入组 24 人开始时间: 2019年2月25日最近更新: 2021年11月1日

试验速览

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•Able to read and comprehend English and give informed consent as demonstrated by signing a record of informed consent;
•Healthy experienced contact lens wearers aged 18 to 45 years of age (inclusive);
•Willing to refrain from using any eye drops and/or contact lenses 24 hours prior to each study visit;
•Spherical Refractive error between +6.00 and -8.00D (inclusive) with cylinder power less than or equal to 0.75D;
•Can attain good vision: Best corrected visual acuity of 6/9.5 or better in each eye;
•Willing to be fitted with and wear mini-scleral contact lenses for the duration of the study visits;
•Willing to attend the scheduled study visits and adhere to instructions.

•Patients who are currently using topical ocular medication or have used topical ocular medication within 2 weeks of the first visit. Patients who are being treated bilaterally with a marketed artificial tear for dry eye can be considered, provided they discontinue use for 24 hours prior to each visit;
•Any contraindications to safe contact lens wear;
•Any systemic disease that may affect ocular health e.g. Graves disease, and auto-immune diseases such as ankylosing spondylitis, multiple sclerosis and systemic lupus erythematosus;
•History of eye surgery within 6 months prior to enrolment in the study;
•Any known allergy to the ingredients in Systane Complete, Systane Hydration, saline and/or the lens disinfecting/conditioning solution.

发起方

SW Sydney