Patient Satisfaction With Contoura Vision Topography-Guided LASIK

Not Applicable

Completed

• Conditions: Myopia; Astigmatism
• Interventions: Procedure: Contoura Vision LASIK

• Registration Number: NCT04903301
• Lead Sponsor: Rush Eye Associates

Brief Summary

To evaluate patient reported outcomes associated with quality of vision before and after treatment with Contoura Vision Topography-Guided LASIK.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-05-21
• Study First Submitted: 2021-05-21
• Study First Submitted QC: 2021-05-21
• Study First Posted: 2021-05-26
• Status Verified: 2023-11
• Primary Completion: 2023-11-01
• Study Completion: 2023-11-01
• Last Update Submitted: 2023-11-15
• Last Update Posted: 2023-11-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Study Group	Contoura Vision LASIK	Contoura Vision LASIK using Phorcides Analytic Software

Primary Outcome Measures

Name	Time	Method
Global Vision Satisfaction Index	26 weeks	Analog Score from Adapted from PROWL Survey

Secondary Outcome Measures

Name	Time	Method
Vision	26 weeks	Uncorrected Visual Acuity using ETDRS
Higher Order Corneal Aberrations	26 weeks	Galilei Topography
Objective Scatter Index	26 weeks	HD Analyzer

Trial Locations

Locations (1)

Rush Eye Associates; 🇺🇸 Amarillo, Texas, United States