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IC-8 Apthera IOL New Enrollment Post Approval Study

← catalyst calendar

NCT06060041 · 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
DateFiledBasisWhat it is
Start2023-09-08actualWhen the study began enrolling
Primary completion2027-09-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-09-30estimatedThe whole study's end, after follow-up
First posted2023-09-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-12actualThe 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 OF
Rate 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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