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A Study to Investigate the Safety and Effectiveness of the Technolas® TENEO 317 Model 2 Excimer Laser for Laser In Situ Keratomileusis (LASIK) Surgery to Treat Myopia or Myopic Astigmatism

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NCT07377474 · readout ≤ 406 d

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

Phase
Not applicable
Status
Not yet recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
32estimated

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
StartApr 2026estimatedWhen the study began enrolling
Primary completionSep 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2027estimatedThe whole study's end, after follow-up
First posted2026-01-30actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-30actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Myopic Astigmatism

Intervention

  • Device: TENEO 317 Model 2 (1.28 US) Excimer Laser

Primary outcomes

what the primary-completion date above is the date OF
The percentage of eyes that achieve predictability (attempted versus achieved) of MRSE within ± 0.50 D
measured Assessed for approximately 12 months
The percentage of eyes that achieve predictability (attempted versus achieved) of MRSE within ± 1.00 D
measured Assessed for approximately 12 months
The percentage of eyes that achieve a UDVA of 20/40 or better
measured Assessed for approximately 12 months

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