Skip to content
KStart free
AI InfrastructureDefenseQuantumAll studies →

1-Week Dispensing Evaluation of REVIVE™ Toric Soft Contact Lenses

← catalyst calendar

NCT06053736 · results posted

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

Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Na · None · Other
Enrollment
32actual
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
Start2023-10-04actualWhen the study began enrolling
Primary completion2023-12-15actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2023-12-15actualThe whole study's end, after follow-up
First posted2023-09-26actualWhen this record first appeared on the registry
Results posted2026-08-25actualWhen the sponsor posted results to the registry
Record updated2026-08-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Refractive Ametropia
  • Astigmatism

Intervention

  • Device: REVIVE Toric Soft Contact Lenses — also filed as REVIVE™ (hioxifilcon D)

Primary outcome

what the primary-completion date above is the date OF
Mean logMAR Visual Acuity at 6m
measured 1-Week Follow-up Visit (approximately 7 ± 3 days after the dispensing visit)

Posted documents

hosted by the registry — we link, never re-serve
Study Protocol and Statistical Analysis Planposted 2023-09-08 · 1005 KB · Prot_SAP_000.pdf

Permalink · BLCO's whole pipeline · Catalyst calendar · Every registered study · What changed