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1-Week Dispensing Evaluation of Kalifilcon A Daily Disposable Multifocal Compared to Ultra for Presbyopia

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NCT05325931 · results posted

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

Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
30actual
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
Start2022-02-25actualWhen the study began enrolling
Primary completion2022-03-28actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2022-03-28actualThe whole study's end, after follow-up
First posted2022-04-13actualWhen this record first appeared on the registry
Results posted2026-08-06actualWhen the sponsor posted results to the registry
Record updated2026-08-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Presbyopia

Interventions

  • Device: kalifilcon A Daily Disposable Multifocal
  • Device: samfilcon A for Presbyopia

Primary outcomes

what the primary-completion date above is the date OF
Visual Acuity (Distance)
measured One week (follow-up visit)
Visual Acuity (Near)
measured One week (follow-up)

Posted documents

hosted by the registry — we link, never re-serve
Study Protocol and Statistical Analysis Planposted 2022-02-07 · 1.2 MB · Prot_SAP_000.pdf

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