Indiana University
Bloomington, Indiana, 47405, United States
NCT Number: NCT07276347
The aim of this study is to assess contact lens performance and acceptance.
Looking for future studies?
Notify Me18 year–45 year
All sexes
Interventional
Not applicable
Bloomington, Indiana, 47405, United States
The objective of this study is to assess the initial performance and acceptance of a range of contact lenses in habitual soft contact lens wearers.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: At the end of 10 hours of daily wear at dispensing
High contrast, high luminance binocular distance visual acuity (logMAR) will be measured at 10-hour visit.
CooperVision International Limited (CVIL)
Industry
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06758076
Eye Diseases, Hyperopia
Manchester, United Kingdom
View Trial DetailsNCT06869044
Eye Diseases, Hyperopia
Berkeley, California, United States
View Trial DetailsNCT06873048
Astigmatism, Eye Diseases
Waterloo, Ontario, Canada
View Trial DetailsNCT05254587
Cataract, Eye Diseases
Bakersfield, California, United States
View Trial Details