Lotrafilcon B contact lens
DeviceCommercially marketed, silicone hydrogel, spherical contact lens having a recommended replacement schedule of monthly.
NCT Number: NCT01007916
The purpose of this study is to compare the performance of commercially marketed contact lenses to habitual contact lenses in a selected segment of the contact lens wearing population.
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Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Commercially marketed, silicone hydrogel, spherical contact lens having a recommended replacement schedule of monthly.
Habitual soft spherical contact lens having a recommended replacement schedule of 2 weeks or monthly.
Time frame: 4 weeks of wear
Comfort upon insertion, as interpreted by the participant, was recorded on a questionnaire by the participant using a 10-point scale, with 1 being poor and 10 being excellent. Comfort upon insertion was assessed as a single, retrospective evaluation of 4-weeks' wear time.
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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.
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