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Clinical trialNCT03918408RecruitingPhase 1Interventional

Safety and Effectiveness of the PXL-Platinum 330 System for Corneal Cross-Linking

SponsorPacific Clear Vision InstituteEnrollment300Bacterial KeratitisEctasia of CorneaKeratoconus, Unstable
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

To determine whether the Peschke PXL-330 system is safe and effective in the treatment of corneal thinning conditions.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

1 registered facility, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Pacific Clear Vision Institute

    Eugene, Oregon, United States

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
1 Sept 2019
Primary completion
31 Dec 2029
Completion
31 Dec 2030
Last update posted
12 Nov 2024
Registered enrollment
300
Registry id
NCT03918408

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.