Performance of Aspheric Hydrogel Lenses After a Refit With Sphere Silicone Hydrogel Lenses for 4 Weeks - Trial NCT03835078
Access comprehensive clinical trial information for NCT03835078 through Pure Global AI's free database. This phase not specified trial is sponsored by Coopervision, Inc. and is currently Completed. The study focuses on Ametropia. Target enrollment is 42 participants.
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Study Focus
Sponsor & Location
Coopervision, Inc.
Timeline & Enrollment
N/A
Jan 01, 2019
Jul 06, 2019
Primary Outcome
Percentage of Participants With Lens Centration Assessment by the Investigator - Methafilcon A Contact Lenses,Percentage of Participants With Lens Centration Assessment by the Investigator - Methafilcon A Contact Lenses,Percentage of Participants With Lens Centration Assessment by the Investigator - Fanfilcon A Contact Lenses,Percentage of Participants With Lens Centration Assessment by the Investigator - Fanfilcon A Contact Lenses,Percentage of Participants With Lens Centration Assessment by the Investigator - Fanfilcon A Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Methafilcon A Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Methafilcon A Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Fanfilcon A Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Fanfilcon A Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Fanfilcon A Contact Lenses,Post-blink Movement Assessment by the Investigator - Methafilcon A Contact Lenses,Post-blink Movement Assessment by the Investigator - Methafilcon A Contact Lenses,Post-blink Movement Assessment by the Investigator - Fanfilcon A Contact Lenses,Post-blink Movement Assessment by the Investigator - Fanfilcon A Contact Lenses,Post-blink Movement Assessment by the Investigator - Fanfilcon A Contact Lenses,Lens Tightness Assessment by the Investigator - Methafilcon A Contact Lenses,Lens Tightness Assessment by the Investigator - Methafilcon A Contact Lenses,Lens Tightness Assessment by the Investigator - Fanfilcon A Contact Lenses,Lens Tightness Assessment by the Investigator - Fanfilcon A Contact Lenses,Lens Tightness Assessment by the Investigator - Fanfilcon A Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Methafilcon A Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Methafilcon A Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Fanfilcon A Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Fanfilcon A Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Fanfilcon A Contact Lenses
Summary
The aim of this prospective study is to evaluate the clinical performance of habitual wearers
 of methafilcon A aspheric lenses after a refit with fanfilcon A sphere lenses for 4 weeks of
 daily wear.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT03835078
Device Trial