NCT04527978.
Methods | RCT, cross‐over design |
Participants |
Inclusion criteria: aged 18 years and older; successful wear of spherical SCL in both eyes for a minimum of 5 days per week and 10 hours per day during the past 3 months; willing to wear contact lenses for at least 16 hours per day Exclusion criteria: ocular condition that contraindicates contact lens wear; previous or current habitual wearer of study contact lenses |
Interventions | Verofilcon A
Nesofilcon A
|
Outcomes |
Primary outcomes:
Secondary outcomes: not specified |
Notes | Sponsorship source: Alcon Research Author's name: CDMA Project Lead, Vision Care Institution: Alcon Research LLC Comments: whether the analysis accounted for cross‐over design was unclear |