IC-8 Apthera IOL New Enrollment Post Approval Study
← catalyst calendarNCT06060041 · readout in 407 d
Sponsored by Bausch & Lomb Incorporated (industry) · BLCO — their whole pipeline →.
Phase
—
Status
Recruiting
Study type
Observational
Enrollment
435estimated
Sites
14
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 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2023-09-08 | actual | When the study began enrolling |
| Primary completion | 2027-09-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-09-30 | estimated | The whole study's end, after follow-up |
| First posted | 2023-09-29 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-01-12 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Cataract
- Presbyopia
- Posterior Capsule Opacification
Primary outcomes
what the primary-completion date above is the date OFRate of any additional Nd:YAG laser treatments beyond the initial Nd:YAG laser treatment
measured 24 Months post IC-8 Apthera IOL Implantation
Nd:YAG laser treatment outcome and/or complications
measured 24 Months post IC-8 Apthera IOL Implantation
IOL related assessments
measured 24 Months post IC-8 Apthera IOL implantation
Rates of Secondary Surgical Interventions (SSIs)
measured 24 Months post IC-8 Apthera IOL implantation
Rates of other serious adverse events
measured 24 Months post IC-8 Apthera IOL implantation
Rates of ocular adverse events
measured 24 Months post IC-8 Apthera IOL implantation
Rates of subjective visual disturbances per the Quality of Vision (QoV) Questionnaire
measured 24 Months post IC-8 Apthera IOL implantation
Rates of subjective visual disturbances per the Small Aperture Patient Questionnaire (SAPQ)
measured 24 Months post IC-8 Apthera IOL implantation
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