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Multicentric Clinical Investigation to Assess Safety and Performance of Lux HighAdd IOL

Study acronym: HIGHADD
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date: Mar 1, 2026 to Sep 2028
    • Study sites: 2 to 3
    • Study completion date: Jul 1, 2026 to Dec 2028
    • Study title expanded, about 1 word
    v3
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Sep 1, 2024 to Dec 19, 2024
    • Site details revised at 2 of 2 sites
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The study purpose is to demonstrate safety and performance of bilateral implantation of LuxHighAdd intraocular lens compared with the LuxGood Monofocal lens.
Trial Details
NCT Number NCT06446817
Lead Sponsor Cutting Edge SAS
Conditions
(from sponsor)		 Cataract
Related terms Cataract
Enrollment 57 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov