CONTOURA vs WFO Ablation PRK & LASIK

Part of paid clinical trials in San Antonio, Texas.

Sponsor
59th Medical Wing
Study ID
NCT05037370
Status
Recruiting

Conditions

  • Refractive Surgery

Eligibility Criteria

Sex
ALL
Age
21 Years - 50 Years
Healthy Volunteers
Accepted

Interventions

  • Wave-Front Optimized (WFO) ablation vs Topography-guided (TG) ablation — DEVICE
    Patient will undergo PRK or LASIK using WFO ablation in one eye and TG ablation on contralateral eye

Study Details

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.

Key Dates

Start date
Apr 22, 2021
Status verified
Aug 2025
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
400 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: LASIK refractive surgery
    Contralateral Randomize Wave-Front Optimized (WFO) ablation vs Topography-guided ablation
  • Experimental: PRK refractive surgery
    Contralateral Randomize Wave-Front Optimized (WFO) ablation vs Topography-guided ablation

Primary Outcome Measure

Post-operative refractive error [ Time Frame: 6 months post-surgery ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Joint Warfighter Refractive Surgery Center at WHASCSan AntonioTexas78236
JOSE E CAPO-APONTE, OD, PhD
210-292-2554
AMBER MARTIN
210-292-2483

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