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Surface Refractive Index Shift of Kalifilcon A Compared With Dailies Total1 and Precision1 Lenses

← catalyst calendar

NCT04840563 · results posted

Sponsored by Bausch & Lomb Incorporated (industry) · BLCO — their whole pipeline →.

Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Na · None · Basic science
Enrollment
10actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-25

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-04-07actualWhen the study began enrolling
Primary completion2021-04-15actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2021-04-15actualThe whole study's end, after follow-up
First posted2021-04-12actualWhen this record first appeared on the registry
Results posted2026-08-05actualWhen the sponsor posted results to the registry
Record updated2026-08-05actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Contact Lens Wear

Interventions

  • Device: kalifilcon A daily disposable spherical soft contact lens — also filed as Infuse
  • Device: Dailies Total1 (delefilcon A) daily disposable spherical soft contact lens
  • Device: Precision1 (verofilcon A) daily disposable spherical soft contact lens

Primary outcome

what the primary-completion date above is the date OF
Surface Refractive Index of Worn Lenses
measured Unworn lens (baseline) and immediately after 0.5, 1, 3, 5, and 10 minutes of lens wear

Posted documents

hosted by the registry — we link, never re-serve
Study Protocol and Statistical Analysis Planposted 2021-03-16 · 736 KB · Prot_SAP_000.pdf

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