Short-term Study of Myday Sphere and Myday Toric Lenses in Existing Spherical Soft Contact Lenses Wearers With Low Astigmatism (Pacific)

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The primary objective of the study is to evaluate and compare the performance of two soft contact lens.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 17
Maximum Age: 42
Healthy Volunteers: f
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• At least 17 years and no more than 42 years of age.

• Have read and signed the study consent form.

• Are willing and able to follow instructions and maintain the appointment schedule.

• Are habitual wearer of spherical soft contact lenses (not toric or multifocal design), any brand and any replacement frequency.

• Are willing to wear the study contact lenses for 6 days a week while in this study and on three days (day 1, Day 7 and Day 13) for at least 12 hours.

• Are willing to provide a contact email and telephone number and to use a device that allows them to respond to a short online questionnaire every 3 hours on days 1, 7 and 13 of each lens arm, while wearing one of the 2 study lenses.

• Are non-presbyopic i.e. no requirement for a reading addition for routine daily tasks (self report).

• Have astigmatism of either -0.50, -0.75, -1.00 or -1.25 DC in each eye by subjective sphero-cylindrical refraction.

• Achieves at least 0.10 LogMAR in each eye by subjective sphero-cylindrical refraction.

⁃ Can be fit with available study contact lens powers of between +6.00 to -10.00 DS.

⁃ Demonstrate an acceptable fit with the study contact lenses.

Locations
Other Locations
Canada
School of Optometry & Vision Science
RECRUITING
Waterloo
Contact Information
Primary
Percy Lazon, PhD
plazon@coopervision.com
+19252516682
Time Frame
Start Date: 2025-02-26
Estimated Completion Date: 2025-08-15
Participants
Target number of participants: 30
Treatments
Experimental: Control Contact Lens (stenfilcon A Sphere)
All participants will wear Control Contact Lens for one week (Period 1).
Experimental: Test Contact Lens (stenfilcon A Toric)
All participants will wear Test Contact Lens for one week (Period 2).
Related Therapeutic Areas
Sponsors
Collaborators: Centre for Ocular Research & Education, Canada
Leads: CooperVision International Limited (CVIL)

This content was sourced from clinicaltrials.gov