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Customized Laser Ablation: Comparing Results of LADAR Vision and VISX Platforms

NCT00344838 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 458

Last updated 2018-01-30

No results posted yet for this study

Summary

To compare the results of two commercially available customized laser ablation devices.

Conditions

  • Customized Laser Ablation

Interventions

DEVICE

Comparison of LADAR CustomLasik and VISX Wavefront System custom laser ablation devices

Sponsors & Collaborators

  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • James P. McCulley, M.D. · University of Texas, Southwestern Medical Center at Dallas

Eligibility

Min Age
18 Years
Max Age
88 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-09-30
Primary Completion
2015-12-31
Completion
2017-10-30

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 NCT00344838 on ClinicalTrials.gov