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CONTOURA vs WFO Ablation PRK & LASIK

RecruitingNAAges 21 Years - 50 YearsAll59th Medical Wing
NCT05037370 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This is a prospective randomized contralateral double-masked study. Each patient will be randomized as to which eye undergoes wave-front optimized (WFO) vs. wave-front guided (WFG) during Photorefractive keratectomy (PRK) or Laser-assisted in situ Keratomileusis (LASIK) surgery to determine which ablation profile provides the best visual outcome.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Meet requirements for PRK or LASIK i.e., Stable \<= .5 D change MRSE) * DOD beneficiaries age 21-50 years * Local pts (w/i 60 mi) who will be in the area for at least 6 months post surgery * Willing to complete all required follow-up visits Exclusion Criteria: * No meeting requirements for PRK or LASIK * Desiring monovision treatment * Anisometropia \>2D spherical equivalent * Prior ocular surgeries / trauma / problem * History of dry eyes * Hyperopia * Mixed astigmatism * Inability to capture VARIO topolyzer scans * Pregnant (or who plans to be within 6 months after surgery) * Breastfeeding any time during the study * History of herpetic disease
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What it tests

  • Wave-Front Optimized (WFO) ablation vs Topography-guided (TG) ablation
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Where

1 site
Joint Warfighter Refractive Surgery Center at WHASC
San Antonio, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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