At a glance
ClinicalIndex Comparison RecordN/ACompleted· 77 enrolled
Drug / intervention
STAR S4IR LASIK with iDesign Aberrometerdevice
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.
A Prospective Study to Evaluate the Performance and Acceptability of the iDesign Advanced WaveScan Study(tm) System
In Brief
A clinical study evaluating STAR S4IR LASIK with iDesign Aberrometer for Refractive Error. Completed, enrolled 77 participants across 4 sites.
Detailed Summary
The results of this trial will demonstrate that the iDesign System performs as intended and is acceptable in a clinical setting.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Error
CountriesCanada
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartOct 2010
First PostedOct 2010
Primary CompletionJun 2011
Study CompletionDec 2011
TodayJul 2026
First PostedOct 14, 2010
Enrollment StartOct 1, 2010
Primary CompletionJun 1, 2011
Study CompletionDec 1, 2011
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 15.7 years ago
Interventions
STAR S4IR LASIK with iDesign Aberrometerdevice
CustomVue LASIK targeted for emmetropia