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.
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