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Excimer Laser
Topography-guided LASIK for Near-sightedness
Phase 3
Waitlist Available
Research Sponsored by Clinical Research Consultants, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Summary
This purpose of this study is to evaluate the safety and effectiveness of a topography-based custom ablation treatment using the ALLEGRETTO WAVE® Eye-Q 400 Hz laser system for treating myopia and hyperopia.
Eligible Conditions
- Near-sightedness
- Farsightedness
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Side effects data
From undefined Phase 3 trial • 212 Patients • NCT010283781%
BSCVA loss of 2 or more lines
1%
Retinal Detachments
100%
80%
60%
40%
20%
0%
Study treatment Arm
Topography-guided LASIK
Trial Design
1Treatment groups
Experimental Treatment
Group I: Topography-guided LASIKExperimental Treatment1 Intervention
Topography-guided LASIK for Myopia or Hyperopia
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
T-CAT topography-guided LASIK treatment with the Allegretto Wave Eye-Q 400 Hz Excimer Laser
2009
Completed Phase 3
~220
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Who is running the clinical trial?
Clinical Research Consultants, Inc.Lead Sponsor
6 Previous Clinical Trials
1,192 Total Patients Enrolled
WaveLight AGIndustry Sponsor
1 Previous Clinical Trials
144 Total Patients Enrolled
Alcon ResearchIndustry Sponsor
728 Previous Clinical Trials
128,842 Total Patients Enrolled
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