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RECRUITING NA

A Three-Phase Contralateral Comparison of Ray-Tracing Guided LASIK Versus Three Other Refractive Surgery Platforms to Correct Myopia or Myopia With Astigmatism

NCT07201298 · View on ClinicalTrials.gov ↗

Study Summary

This purpose of this study is to compare a new form of LASIK called Ray Tracing Guided LASIK to 3 other forms of corneal refractive surgery: 1. KLEx (KeratoLenticule Extraction) using the Zeiss Visumax 800 Laser, 2. WFO LASIK (Wavefront Optimized LASIK) using the Alcon EX500 Laser, and 3. Topography Guided LASIK (Contoura LASIK) also using the Alcon EX500 Laser.

Conditions Studied

Interventions

  • DEVICE Ray-Tracing Guided LASIK
  • DEVICE Keratorefractive Lenticule Extraction (KLEx)
  • DEVICE WaveFront Optimized LASIK
  • DEVICE Topography Guided LASIK

Study Locations (1)

Utah

  • Hoopes Moshirfar Research Center — Draper

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2025-09
Est. Completion 2029-09
Phase NA

Sponsor

Hoopes Vision

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07201298

The ClinicalTrials.gov registry entry for NCT07201298 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoopes Vision, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Myopia appearing as the primary indexed condition, and to 4 interventions — of which Ray-Tracing Guided LASIK is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07201298 reports 1 study location spanning 1 distinct geographic area — top geographies include Utah. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07201298 about?

NCT07201298 is a clinical study titled "A Three-Phase Contralateral Comparison of Ray-Tracing Guided LASIK Versus Three Other Refractive Surgery Platforms to Correct Myopia or Myopia With Astigmatism". This purpose of this study is to compare a new form of LASIK called Ray Tracing Guided LASIK to 3 other forms of corneal refractive surgery: 1. KLEx (KeratoLenticule Extraction) using the Zeiss Visumax 800 Laser, 2. WFO LASIK (Wavefront Optimized LASIK) using the Alcon EX500 Laser, and 3. Topography...

What is the current status of trial NCT07201298?

This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2025-09. Estimated completion is 2029-09.

What conditions does trial NCT07201298 study?

This clinical trial studies the following conditions: Myopia, Astigmatism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07201298?

The interventions under investigation include: Ray-Tracing Guided LASIK (DEVICE), Keratorefractive Lenticule Extraction (KLEx) (DEVICE), WaveFront Optimized LASIK (DEVICE), Topography Guided LASIK (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07201298?

This trial is sponsored by Hoopes Vision, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07201298 being conducted?

This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial