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Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure

NCT01061294 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2011-01-13

No results posted yet for this study

Summary

The purpose of this study is to assess the efficacy, predictability and safety of the Advanced CustomVue™ iLASIK procedure (WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System). Patient data will be collected electronically and analyzed to determine improvements in postoperative visual acuity, visual quality and residual error.

Conditions

  • Vision Correction

Interventions

PROCEDURE

Advanced CustomVue™ iLASIK procedure

DEVICE

WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System

Sponsors & Collaborators

  • Innovative Medical

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2010-12-31
Completion
2010-12-31

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 NCT01061294 on ClinicalTrials.gov