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Patient Satisfaction With Contoura Vision Topography-Guided LASIK

Sponsored by Rush Eye Associates

About this trial

Last updated 2 years ago

Study ID

CV-LASIK

Status

Completed

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
21 to 35 Years
All
All

Trial Timing

Ended 2 years ago

What is this trial about?

To evaluate patient reported outcomes associated with quality of vision before and after treatment with Contoura Vision Topography-Guided LASIK.

What are the Participation Requirements?

Eligibility criteria: The study enrollment will include all willing patients with:
pre-operative BCVA 20/20 for each eye individually, myopic refractive error up to -8.00
diopters, refractive astigmatism that ranges from 0 to 3 diopters, maximum spherical
equivalent of -9.00 diopters, the designated age requirements, and only patients that
have signed the informed consent document.

Exclusion criteria: Patients are excluded that are not willing to participate in a
research trial, are unable to cooperate well enough to safely perform the procedure, fail
to meet inclusion criteria, have ocular disease (including but not limited to
keratoconus, macular degeneration, glaucoma, corneal dystrophy, dry eye syndrome and
corneal scarring), and patients that have had previous ocular surgery. Any patients with
known allergies to the post-operative medications or preservatives in the medications
will also be excluded.

Locations

Location

Status