Lotrafilcon A contact lens
DeviceSilicone hydrogel contact lens
NCT Number: NCT00810511
The purpose of this trial is to compare two different contact lenses during 4 weeks of wear.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Silicone hydrogel contact lens
Silicone hydrogel contact lens
Time frame: After 4 weeks of wear
Evaluated by the subject as a single, retrospective evaluation of 4-week wear time. Measured on a 10-point scale, with 1 being poor and 10 being excellent.
CIBA VISION
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.
NCT07284966
Astigmatism, Eye Diseases
San Diego, California, United States
View Trial DetailsNCT06817785
Eye Diseases, Myopia
Waterloo, Ontario, Canada
View Trial DetailsNCT07780851
Eye Diseases, Myopia
Singapore
View Trial DetailsNCT06884202
Eye Diseases, Myopia
Los Angeles, California, United States
View Trial Details