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Clinical Investigation of a Femtosecond Laser for Corneal Flap Creation

NCT07036835 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2026-04-13

No results posted yet for this study

Summary

The purpose of this study is to see how safe the WaveLight Ultraviolet Femtosecond Laser, Model 1026 (UV fs-Laser), is for creating corneal flaps during laser-assisted in situ keratomileusis (LASIK) surgery. This study will be conducted in Australia.

Conditions

  • Refractive Errors

Interventions

PROCEDURE

LASIK Surgery

Laser assisted in situ keratomileusis (LASIK) surgery conducted for the purpose of correcting refractive error

DEVICE

UV fs-Laser

WaveLight Ultraviolet Femtosecond Laser used for creating a corneal flap during LASIK surgery

DEVICE

IR fs-Laser

WaveLight FS200 Infrared Femtosecond Laser used for creating a corneal flap during LASIK surgery

DEVICE

Anesthetic 1 eye drops

Topical anesthetic used to numb the surface of the eye

DEVICE

Anesthetic 2 eye drops

Topical anesthetic used to numb the surface of the eye

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Trial Lead, 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
2025-08-27
Primary Completion
2026-07-31
Completion
2026-07-31

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 NCT07036835 on ClinicalTrials.gov