Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure

Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure (Wavescan Wavefront® System, Star S4 IR™ Excimer Laser System and Intralse™ FS System)

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.

Study Overview

• Status: Completed
• Conditions: Vision Correction
• Intervention / Treatment: Procedure: Advanced CustomVue™ iLASIK procedure; Device: WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System

• Study Type: Interventional
• Enrollment (Anticipated): 20
• Phase: Phase 4

Contacts and Locations

Study Locations

• United States
  • Florida
    • Miami, Florida, United States, 33176
      • William Trattler

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 21 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. the subject must be male or female, of any race, and at least 21 years old at the time of the pre-operative examination;
2. both eyes must have a BSCVA of 20/20 or better;
3. both eyes must have a manifest refractive error from -0.50 D to -6.00 D, a cylinder component up to -3.00 D, and a maximum manifest spherical equivalent of -6.00 D;
4. both eyes must have a minimum pupil size of at least 6.0mm in dim illumination on wavescan;
5. both eyes must demonstrate refractive stability confirmed by clinical records or previous glasses. Refractive stability shall be documented by a change of less than or equal to 0.50 diopter (sphere and cylinder) at an exam at least 12 months prior to the baseline examination. The astigmatic axis must also be within 15 degrees for eyes with cylinder greater than 0.50 D; and
6. subjects should be willing and capable of returning for follow-up examinations for the duration of the study.

Exclusion Criteria:

1. subjects who use concurrent topical or systemic medications that may impair healing, including but not limited to: antimetabolites, isotretinoin (Accutane®) within 6 months of treatment, and amiodarone hydrochloride (Cordarone®) within 12 months of treatment; NOTE: The use of topical or systemic corticosteroids, whether chronic or acute, is deemed to adversely affect healing and subjects using such medication are specifically excluded from eligibility.
2. subjects with a history of any of the following medical conditions, or any other condition that could affect wound healing: collagen vascular disease, autoimmune disease, immunodeficiency diseases, ocular herpes zoster or simplex, endocrine disorders (including, but not limited to unstable thyroid disorders and diabetes), lupus, and rheumatoid arthritis; NOTE: The presence of diabetes (either type 1 or 2), regardless of disease duration, severity or control, will specifically exclude subjects from eligibility.
3. the subject must not have a history of prior intraocular or corneal surgery (including cataract extraction), active ophthalmic disease or abnormality (including, but not limited to, blepharitis, recurrent corneal erosion, dry eye syndrome, neovascularization > 1mm from limbus), clinically significant lens opacity, clinical evidence of trauma (including scarring), or with evidence of glaucoma or propensity for narrow angle glaucoma in either eye; NOTE: This includes any subject with open angle glaucoma, regardless of medication regimen or control. .
4. the subject must not have any evidence of keratoconus, corneal irregularity, or abnormal videokeratography in either eye;
5. subjects with known sensitivity or inappropriate responsiveness to any of the medications used in the post-operative course;
6. patients who do not achieve Iris registration at the time of their wavescan; and
7. patients seeking monovision.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Advanced CustomVue™ iLASIK procedure	Procedure: Advanced CustomVue™ iLASIK procedure; Device: WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Postoperative visit procedures will include visual acuity and quality assessments and monitoring for surgical complications necessitating retreatment.	1 year

Collaborators and Investigators

• Sponsor: Innovative Medical

Study record dates

Study Major Dates

• Study Start: December 1, 2009
• Primary Completion (Actual): December 1, 2010
• Study Completion (Actual): December 1, 2010

Study Registration Dates

• First Submitted: February 1, 2010
• First Submitted That Met QC Criteria: February 2, 2010
• First Posted (Estimate): February 3, 2010

Study Record Updates

• Last Update Posted (Estimate): January 13, 2011
• Last Update Submitted That Met QC Criteria: January 12, 2011
• Last Verified: January 1, 2011

More Information

Terms related to this study

• Keywords: Assess the efficacy, predictability and safety of the Advanced CustomVue™ iLASIK procedure.
• Other Study ID Numbers: iLASIK