At a glance
ClinicalIndex Comparison RecordN/ACompleted· 200 enrolled
Drug / intervention
IntraLase iFS femtosecond laser and patient interface +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.
A Prospective, Multi-Center Evaluation of Corneal Flap Creation Using Cheetah Femtosecond Laser System and Cheetah Patient Interface
In Brief
A clinical study evaluating IntraLase iFS femtosecond laser and patient interface and Cheetah femtosecond laser and cheetah patient interface for Refractive Error. Completed, enrolled 200 participants across 3 sites in 2 countries.
Detailed Summary
The study is a prospective, open-label, comparative study design that was chosen for the purpose of optimizing the Cheetah settings, and evaluating the Cheetah system quality of LASIK flap.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Error
CountriesIndia, Singapore
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartDec 2018
First PostedDec 2018
Primary CompletionMar 2023
TodayJul 2026
First PostedDec 28, 2018
Enrollment StartDec 19, 2018
Primary CompletionMar 31, 2023
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 7.5 years ago
Interventions
IntraLase iFS femtosecond laser and patient interfacedevice
Commercial ophthalmic laser surgical system
Cheetah femtosecond laser and cheetah patient interfacedevice
Ophthalmic laser surgical system