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Evaluation of the Post-LASIK Flap Thickness of the FS200 Femtosecond Laser Flap

NCT01693939 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2013-01-25

No results posted yet for this study

Summary

The purpose of this study is to document the programmed flap thickness to achieved flap thickness using the FS200 femtosecond laser in performing LASIK procedure. The FS200 Femtosecond laser is a precision surgical device that is used to create a flap in a FDA approved LASIK procedure.

Conditions

  • Myopia

Interventions

DEVICE

FS200 Femtosecond Laser

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Durrie Vision

    lead OTHER

Principal Investigators

  • Daniel S. Durrie, MD · Durrie Vision

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2012-04-30
Completion
2012-04-30

Countries

  • United States

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 NCT01693939 on ClinicalTrials.gov