NCT04908488.
Methods | RCT, cross‐over design |
Participants |
Inclusion criteria: aged 18 years and older; successful wear of toric 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 study contact lenses for at least 16 hours per day Exclusion criteria: habitual wear of study contact lenses; spherical monovision or multifocal lens wearer; habitual contact lenses when sleeping for at least 1 night per week over 3 months prior to enrollment |
Interventions | Verofilcon A
Etafilcon A
|
Outcomes |
Primary outcome:
Secondary outcome: not specified |
Notes | Sponsorship source: Alcon Research Author's name: Clinical Trial Lead, Vision Care, Alcon Research LLC Institution: Alcon Research LLC Comments: no trial results |