Performance of Toric Hydrogel Lenses Following A Refit With Toric Silicone Hydrogel Lenses for 1 Month - Trial NCT03835221
Access comprehensive clinical trial information for NCT03835221 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 43 participants.
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Study Focus
Sponsor & Location
Coopervision, Inc.
Timeline & Enrollment
N/A
Jan 01, 2019
Jul 06, 2019
Primary Outcome
Number of Participants With Lens Centration Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Number of Participants With Lens Centration Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Number of Participants With Lens Centration Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Number of Participants With Lens Centration Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Number of Participants With Lens Centration Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Percentage of Participants With Corneal Coverage Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Post-blink Movement Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Post-blink Movement Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Post-blink Movement Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Post-blink Movement Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Post-blink Movement Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Lens Orientation in Primary Position of Gaze Assessment by the Investigator - Methalfilcon A Toric Contact Lenses,Lens Orientation in Primary Position of Gaze Assessment by the Investigator - Methalfilcon A Toric Contact Lenses,Lens Orientation in Primary Position of Gaze Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Lens Orientation in Primary Position of Gaze Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Lens Orientation in Primary Position of Gaze Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Rotational Recovery Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Rotational Recovery Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Rotational Recovery Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Rotational Recovery Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Rotational Recovery Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Overall Stability Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Overall Stability Assessment by the Investigator - Methafilcon A Toric Contact Lenses,Overall Stability Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Overall Stability Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Overall Stability Assessment by the Investigator - Fanfilcon A Toric Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Methafilcon A Toric Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Methafilcon A Toric Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Fanfilcon A Toric Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Fanfilcon A Toric Contact Lenses,Overall Lens Fit Acceptance by the Investigator - Fanfilcon A Toric Contact Lenses
Summary
The aim of this prospective study is to evaluate the clinical performance of habitual wearers
 of methafilcon A toric lenses after a refit with fanfilcon A toric lenses for 1-month of
 daily wear.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT03835221
Device Trial