At a glance
ClinicalIndex Comparison RecordN/ACompleted· 33 enrolled
Drug / intervention
FS200 femtosecond laser LASIK +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
LASIK Flap Thickness and Visual Outcomes Using the WaveLight FS200 Femtosecond Laser: 3 Months Follow-up of Initial US Clinical Series
In Brief
A clinical study evaluating FS200 femtosecond laser LASIK and IntraLase femtosecond laser LASIK for Myopia. Completed, enrolled 33 participants across 1 site.
Detailed Summary
The objective of this study is to evaluate the visual outcome, accuracy, predictability and complications of LASIK flap creation using the Alcon Wavelight FS200 Femtosecond laser and compare these results to those obtained using current IntraLase FS60 Femtosecond laser. The primary outcome to be evaluated is the flap thickness accuracy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
CollaboratorsAlcon Research
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartAug 2012
First PostedFeb 2014
Primary CompletionSep 2015
Study CompletionSep 2016
TodayJul 2026
First PostedFeb 12, 2014
Enrollment StartAug 1, 2012
Primary CompletionSep 1, 2015
Study CompletionSep 1, 2016
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 12.4 years ago
Interventions
FS200 femtosecond laser LASIKdevice
IntraLase femtosecond laser LASIKdevice