Contoura With Phorcides Compared to Wavefront Optimized LASIK

Recruiting N/A Interventional Study
Myopia Astigmatism
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
21 – 38
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Daniel Terveen · Other
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About This Trial

Comparing post-operative visual acuity and patient reported satisfaction between Contoura with Phorcides and WaveLight Wavefront Optimized.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients at least age 21 years of age undergoing LASIK eye surgery * Willing and able to comprehend informed consent and complete 1 month post-op visit * Potential postoperative BCDVA of 20/20 or better in each eye based on Investigator's medical opinion * Candidates for Conto…
Contacts

Daniel Terveen, MD

605-645-7999

daniel.terveen@vancethompsonvision.com

CONTACT

Elise Meide, M.S.

605-645-0444

elise.reid@coyotes.usd.edu

CONTACT