Comprehensive Assessment of Multiple Products (CAMP)
NCT07276347 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36
Last updated 2026-04-13
Summary
The aim of this study is to assess contact lens performance and acceptance.
Conditions
- Hyperopia
- Myopia
Interventions
- DEVICE
-
somofilcon A lens
Participants will be randomized to wear somofilcon A soft contact lens for 10 hours.
- DEVICE
-
stenfilcon A lens
Participants will be randomized to wear stenfilcon A soft contact lens for 10 hours.
- DEVICE
-
fanfilcon A lens
Participants will be randomized to wear fanfilcon A soft contact lens for 10 hours.
- DEVICE
-
comfilcon A lens
Participants will be randomized to wear comfilcon A soft contact lens for 10 hours.
- DEVICE
-
verofilcon A lens
Participants will be randomized to wear verofilcon A soft contact lens for 10 hours.
- DEVICE
-
serafilcon A lens
Participants will be randomized to wear serafilcon A soft contact lens for 10 hours.
- DEVICE
-
lehfilcon A lens
Participants will be randomized to wear lehfilcon A soft contact lens for 10 hours.
- DEVICE
-
delefilcon A lens
Participants will be randomized to wear delefilcon A soft contact lens for 10 hours.
- DEVICE
-
senofilcon A daily disposable lens
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
- DEVICE
-
senofilcon A with blue light technology lens
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
- DEVICE
-
senofilcon A bi-weekly lens
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
- DEVICE
-
samfilcon A lens
Participants will be randomized to wear samfilcon A soft contact lens for 10 hours.
- DEVICE
-
kalilfilcon A lens
Participants will be randomized to wear kalifilcon A soft contact lens for 10 hours.
Sponsors & Collaborators
-
CooperVision International Limited (CVIL)
lead INDUSTRY
Principal Investigators
-
Pete Kollbaum, OD, PhD · Indiana University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-11-12
- Primary Completion
- 2025-12-17
- Completion
- 2025-12-17
- FDA Device
- Yes
Countries
- United States
Study Locations
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