NCT05138783.

Methods	RCT, cross‐over design
Participants	Inclusion criteria: age 18 years and older; successful wear of spherical SCL for at least 3 months, with a minimum wearing time of 5 days per week and 10 hours per day; willing to wear contact lenses for at least 16 hours on the day prior to specified visit days Exclusion criteria: participation in a clinical trial within the previous 30 days or currently enrolled in any clinical trial; habitual use of study SCL; habitual monovision or multifocal lens wear
Interventions	Verofilcon A material: silicon hydrogel replacement frequency: daily Nesofilcon A material: hydrogel replacement frequency: daily
Outcomes	Primary outcome: distance VA with study lenses (logMAR) 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