CompletedNot Applicable

Bilateral Dispensing Study of MyDay Toric, 1-day Acuvue Moist for Astigmatism, and Dailies Aquacomfort Plus Toric Lenses

Canada60 participantsStarted 2016-10-19

Plain-language summary

Bilateral dispensing study of MyDay Toric, 1-day Acuvue Moist for Astigmatism, and Dailies Aquacomfort Plus Toric lenses

Age range17 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. Is at least 17 years of age and has full legal capacity to volunteer;
✓. Has had a self-reported oculo-visual examination in the last two years.
✓. Has read and signed an information consent letter;
✓. Is willing and able to follow instructions and maintain the appointment schedule;
✓. Is an adapted soft contact lens wearer;
✓. Is willing to wear contact lens in both eyes for the duration of the study;
✓. Has a minimum spectacle astigmatism of - 0.75;
✓. Can be fit with the three study contact lens types in the powers available;

✕. Is participating in any concurrent clinical trial;
✕. Has any known active\* ocular disease and/or infection;
✕. Has a systemic condition that in the opinion of the investigator may affect a study outcome variable;
✕. Is using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable;
✕. Has known sensitivity to fluorescein dye or products to be used in the study;
✕. Appears to have any active\* ocular pathology, ocular anomaly or severe insufficiency of lacrimal secretion (severe dry eye) that would affect the wearing of contact lenses;
✕. Is pregnant, lactating or planning a pregnancy at the time of enrolment (by verbal confirmation at the screening visit);
✕. Is aphakic;

Comfort

Timeframe: 1 week

Dryness

Timeframe: 1 week

Visual Quality

Timeframe: 1 week

Lens Preference With Respect to Overall Comfort

Timeframe: 1 week

Lens Preference With Respect to Visual Quality

Timeframe: 1 week

NCT IDNCT03134248

SponsorCooperVision, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2017-04-12

Results submitted2018-05-14

Who can participate

Age range17 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. Is at least 17 years of age and has full legal capacity to volunteer;
✓. Has had a self-reported oculo-visual examination in the last two years.
✓. Has read and signed an information consent letter;
✓. Is willing and able to follow instructions and maintain the appointment schedule;
✓. Is an adapted soft contact lens wearer;
✓. Is willing to wear contact lens in both eyes for the duration of the study;
✓. Has a minimum spectacle astigmatism of - 0.75;
✓. Can be fit with the three study contact lens types in the powers available;

✕. Is participating in any concurrent clinical trial;
✕. Has any known active\* ocular disease and/or infection;
✕. Has a systemic condition that in the opinion of the investigator may affect a study outcome variable;
✕. Is using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable;
✕. Has known sensitivity to fluorescein dye or products to be used in the study;
✕. Appears to have any active\* ocular pathology, ocular anomaly or severe insufficiency of lacrimal secretion (severe dry eye) that would affect the wearing of contact lenses;
✕. Is pregnant, lactating or planning a pregnancy at the time of enrolment (by verbal confirmation at the screening visit);
✕. Is aphakic;