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Contralateral Study of WaveLight® Femtosecond Laser Devices for Corneal Flap Creation

NCT06021353 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2024-12-27

No results posted yet for this study

Summary

The purpose of this study is to assess the WaveLight Ultraviolet Femtosecond Laser System, Model 1026 (UV fs-Laser) corneal flap creation accuracy as compared to the already marketed WaveLight FS200 Infrared Femtosecond Laser, Model 1025 (IR fs-Laser).

Conditions

  • Refractive Errors

Interventions

DEVICE

UV fs-Laser

Stationary scanning spot femtosecond laser used for corneal flap creation during refractive surgery

DEVICE

IR fs-Laser

Stationary scanning spot femtosecond laser used for corneal flap creation during refractive surgery

PROCEDURE

LASIK

Laser-assisted in situ keratomileusis (LASIK) surgery

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Principal Clinical Trial Lead, CRD Surgical · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-20
Primary Completion
2024-12-12
Completion
2024-12-12

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06021353 on ClinicalTrials.gov