Accuracy of LASIK Flaps Created With the LenSx® Femtosecond Laser - A Pilot Study
Completed · Not applicable
Conditions studied: Myopia, Hyperopia
In brief
The purpose of this study is to evaluate the thickness accuracy of Laser-assisted in situ keratomileusis (LASIK) flaps created with the LenSx® Laser.
Key facts
- Study ID
- NCT02575911
- Run by
- Alcon Research
- People needed
- 34
- Starts
- 2015-10-28
- Expected to finish
- 2016-04-09
- Last updated by the study team
- 2018-07-02
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with myopia or hyperopia and eligible for femtosecond laser initiated LASIK surgery;
- Best corrected visual acuity (BCVA) correctable to at least 20/25 in each eye;
- If contact lens wearer, willing to discontinue contact lens wear prior to screening procedures;
- Willing and able to return for ALL scheduled follow-up examinations;
- Willing and able to provide written informed consent;
- Eligible for bilateral LASIK procedures to be done on the same day;
- Other protocol-specified inclusion criteria may apply.
You may not qualify if…
- Previous corneal surgery, corneal lesions that will impede laser treatment, corneal edema, hypotony, glaucoma, existing corneal implant, or keratoconus;
- Known sensitivity to planned study concomitant medications;
- Participation in any other ophthalmic drug or device clinical study for 30 days prior to or during the time of participation in this study;
- Irregular astigmatism, based on the Investigator's judgement;
- Pregnant, lactating or planning to become pregnant during the course of the study;
- Other protocol-specified exclusion criteria may apply.
Where it is running
- Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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