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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Myopia
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
Astigmatism is an imperfection in the curvature of the eye's cornea or lens that causes blurry vision. The aim of this study is to find out whether the overall visual performance of the study contact lens with an astigmatic correction is better than the study contact lens without an astigmatic correction.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
To be eligible as a participant, each candidate shall be free of any ocular or medical condition that may affect the results of this study.
The following are specific criteria that exclude a candidate from enrolment in this study:1. Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear2. Newly prescribed (within the past 30 days) use of some systemic medications (such as antihistamines, decongestants, diuretics, muscle relaxants, tranquilizers, stimulants, anti-depressants, anti-psychotics, oral contraceptives) or new prescription eyedrops which is not rewetting/lubricating eyedrops for which contact lens wear could be contraindicated as determined by the investigator3. Monocular participants (only one eye with functional vision) or participants fit with only one lens4. Subjects with slit lamp findings greater than grade 2 or higher (e.g. oedema, infiltrates, corneal neovascularization, corneal staining, tarsal abnormalities, conjunctival, anterior segment inflammation) as per ISO 11980, any previous history or signs of a contact lens related corneal inflammatory event (past corneal ulcers), or any other ocular abnormality that may contraindicate contact lens wear at the enrolment visit5. History of herpetic keratitis, ocular surgery or irregular cornea6. Enrolment of the family members of the investigator, family members of the investigator’s staff, or individuals living in the households of these individuals
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Ms
Deborah
Moore
+44 (0)2072224224
dmoore@otg.co.uk
The study is sponsored by CooperVision International Limited and funded by CooperVision.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
