FDA Clinical Studies

Johnson & Johnson Surgical Vision: STAR-122-MVPM. A Post-approval Study of Wavefront-guided LASIK for Monovision Treatment of Myopic Subjects with Presbyopia. This study is currently enrolling new patients.
(temporarily halt due to COVID-19)

AMO Protocol CRKID-2016-01: A Clinical Study Evaluating the Safety, Efficacy and Patient Satisfaction using the iDesign Advanced Wavescan Studio in the Treatment of Myopic Astigmatism in Individuals Undergoing Bilateral LASIK Surgery. This study is currently closed to new patients.

AMO Investigational Protocol: STAR-110-IDMY. A Prospective Study to Evaluate the Safety and Effectiveness of Wavefront-Guided LASIK Correction of Myopic Refractive Errors with the iDesign Advanced WaveScan Studio™ System and STAR S4 IR™ Excimer Laser System. This study is currently closed to new patients.

ACU-P08-020: A Prospective Multicenter Clinical Trial to Evaluate the Safety and Effectiveness of the AcuFocus Corneal Inlay ACl7000PDT Implanted Intra-Stromally for Modified Monovision in Presbyopic Patients. This study is currently closed to new patients.

AMO Investigational Protocol: STAR-112-IDMA. A Prospective Study to Evaluate the Safety and Effectiveness of Wavefront-Guided LASIK Correction of Mixed Astigmatism Refractive Errors with the iDesign Advanced WaveScan Studio™ System and STAR S4 IR™ Excimer Laser System. This study is currently closed to new patients.