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Clinical Outcomes of the Gore Synthetic Cornea Device

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial status: Recruiting to Active, Not Recruiting
    • Site details revised at 2 of 2 sites
    v7
  2. 2 versions Re-verified since Oct 16, 2024, no change to tracked fieldsv5-v6
  3. Trial status: Not Yet Recruiting to Recruiting
    • Start date: Aug 1, 2024 to Aug 19, 2024
    • Site details revised at 2 of 2 sites
    v4
  4. Start date: Jul 1, 2024 to Aug 1, 2024
    • Study sites: 0 to 2
    v3
  5. Start date: Jan 1, 2024 to Jul 1, 2024v2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Study objective is to evaluate the initial safety and effectiveness of the GORE Synthetic Cornea Device in the treatment of loss of corneal clarity in patients who are candidates for corneal transplantation
Trial Details
NCT Number NCT06174376
Lead Sponsor W.L.Gore & Associates
Conditions
(from sponsor)		 Corneal Opacity
Related terms Corneal Opacity
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov