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LASIK Using Contoura With Phorcides vs. iDesign

NCT07128316 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2025-08-18

No results posted yet for this study

Summary

Participants will undergo LASIK using Contoura with Phorcides calculation on one eye and LASIK using iDesign calculation on the contralateral eye to correct myopia.

Conditions

  • Myopia
  • Astigmatism

Interventions

DEVICE

Contoura Topolyzer with Phorcides

LASIK calculated ablation using Contoura Topolyzer with Phorcides

DEVICE

iDesign

LASIK calculated ablation using iDesign Refractive Studio 2.0

Sponsors & Collaborators

  • 59th Medical Wing

    lead FED

Principal Investigators

  • Samantha B Rodgers, MD · 59th Medical Wing

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-11
Primary Completion
2025-12-15
Completion
2025-12-15
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07128316 on ClinicalTrials.gov