Comprehensive Assessment of Multiple Products (CAMP)
CooperVision International Limited (CVIL)
250 participants
Dec 1, 2025
INTERVENTIONAL
Conditions
Summary
The aim of this study is to assess contact lens performance and acceptance.
Eligibility
Inclusion Criteria5
- Age 18 to 45 years (inclusive)
- Habitual soft spherical contact lens wearer (current prescription)
- Refractive error of -6.00 to -0.50DS or +0.50 to +6.00DS and less than or equal to 0.75DC as vertexed to the corneal plane
- Anisometropia no greater than 1.50D, based on vertexed manifest refraction spherical equivalent
- Can achieve visual acuity of at least 20/25 in each eye with spherical equivalent manifest refraction
Exclusion Criteria4
- Active anterior segment infection, inflammation or abnormality that would contraindicate contact lens wear
- Use of systemic or ocular medication that would contraindicate contact lens wear
- Used gas permeable/hard contact lenses (including orthokeratology) in the previous 3 months
- Participation in a contact lens or lens care product trial in the previous 30 days
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Interventions
Participants will be randomized to wear somofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear stenfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear fanfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear comfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear verofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear serafilcon A soft contact lens for 10 hours.
Participants will be randomized to wear lehfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear delefilcon A soft contact lens for 10 hours.
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear samfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear kalifilcon A soft contact lens for 10 hours.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07276347