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Completed Not applicable Interventional Results available

WaveLight® EX500 Excimer Laser System for the Correction of Myopia Using InnovEyes™ in Conjunction With InnovEyes™ Sightmap

ClinicalTrials.gov ID: NCT04219891

Public ClinicalTrials.gov record NCT04219891. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 1:19 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Pivotal Trial of WaveLight® EX500 Excimer Laser System for the Correction of Myopia With and Without Astigmatism Using InnovEyes™ in Conjunction With InnovEyes™ Sightmap

Study identification

NCT ID
NCT04219891
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Alcon Research
Industry
Enrollment
272 participants

Conditions and interventions

Conditions

Interventions

  • WaveLight EX500 excimer laser system with InnovEyes sightmap Device
  • LASIK Procedure
  • InnovEyes sightmap Device

Device · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 8, 2020
Primary completion
Nov 8, 2022
Completion
Nov 8, 2022
Last update posted
Apr 5, 2025

2020 – 2022

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Alcon Investigative Site San Diego California 92122
Price Vision Group Indianapolis Indiana 46260
Alcon Investigative Site Chevy Chase Maryland 20815-7018
Alcon Investigative Site Kansas City Missouri 64154
Alcon Investigative Site St Louis Missouri 63017
Alcon Investigative Site Omaha Nebraska 68135
Alcon Investigative Site Mt. Pleasant South Carolina 29464
Alcon Investigative Site Sioux Falls South Dakota 57108
Alcon Investigative Site Dallas Texas 75243

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04219891, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 5, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04219891 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →