About this trial
This is a post-market observational clinical investigation. The objective of this observational study is to evaluate the visual performance and HCP satisfaction of REVIVE samfilcon B custom toric contact lenses.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Be 18 years or older on the date the ICF is signed
Have the capacity to read, understand, and provide written voluntary informed consent
Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings
Have no active ocular disease or allergic conjunctivitis
Disqualifiers
Is participating in another research study
Is considered by the Investigator to not be a suitable candidate for participation
Is not eligible for treatment with the study lens per the IFU (contraindicated)
Has had previous ocular surgery
Trial population
Patient population at study site locations
Trial design
Case-only
Prospective
Treatments tested in this trial
REVIVE samfilcon B custom toric contact lenses
DeviceREVIVE samfilcon B custom toric contact lenses
Treatment groups
Trial outcomes
Primary outcomes
Investigator overall satisfaction as assessed by the Investigator Survey
(completed by the Investigator for each subject at 14 days ± 3 days after the final dispensing/refinement visit)
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: