At a glance
ClinicalIndex Comparison RecordN/ACompleted· 167 enrolled
Drug / intervention
STAR S4 IR laser with iDesigndevice
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 Safety and Effectiveness of Wavefront-guided PRK Correction of Myopic Refractive Errors With the iDesign Advanced Wavescan Studio™ System and the Star S4 IR™ Excimer Laser System
In Brief
A clinical study evaluating STAR S4 IR laser with iDesign for Stable Myopic Refractive Error, With or Without Astigmatism. Completed, enrolled 167 participants.
Detailed Summary
Prospective, multicenter, bilaterally-treated, open-label, non-randomized clinical trial.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartFeb 2016
First PostedFeb 2016
Primary CompletionJul 2018
TodayJul 2026
First PostedFeb 5, 2016
Enrollment StartFeb 3, 2016
Primary CompletionJul 27, 2018
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 10.4 years ago
Interventions
STAR S4 IR laser with iDesigndevice
Surgeons will perform wavefront-guided PRK for the treatment of myopic refractive errors based upon measurements obtained with the iDesign System using the STAR S4 IR laser.