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A Comparison of LASIK Outcomes Using Two Femtosecond Lasers

NCT03063164 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2021-12-14

Study results available
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Summary

Comparing LASIK outcomes using two femtosecond lasers

Conditions

  • Myopia
  • Astigmatism

Interventions

DEVICE

Intralase IFS150

Intralase flap creation

DEVICE

Visumax

Visumax flap creation

Sponsors & Collaborators

  • Edward E. Manche

    lead OTHER

Principal Investigators

  • Edward Manche, MD · Stanford University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-14
Primary Completion
2018-11-13
Completion
2018-11-13
FDA Device
Yes

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 NCT03063164 on ClinicalTrials.gov