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The VIS Opti-K Low Vision Aid Device Provides Vision Improvement.

Study acronym: Opti-K Pres
StatusNot Yet Recruiting
PhaseNot applicable
SponsorVIS, Inc.
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated September 25, 2024 (before its estimated September 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Site contacts updated at 2 of 2 sites
    • Study title revised
    v2
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
VIS, Inc.
4 trials monitored
See all monitored trials
The VIS Opti-K Low Vision Aid device will be used to provide vision improvement to patients with refractive disorders (hyperopia and presbyopia).
Trial Details
NCT Number NCT06597292
Lead Sponsor VIS, Inc.
Conditions
(from sponsor)		 Hyperopia, Presbyopia
Related terms Hyperopia, Presbyopia
Enrollment 200 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov