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Completed Not applicable Interventional Results available

A Study With Technolas® TENEO 317 Model 2 Excimer Laser to Treat Participants With Myopia or Myopic Astigmatism

ClinicalTrials.gov ID: NCT04111757

Public ClinicalTrials.gov record NCT04111757. 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 21, 2026, 12:38 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

A Study to Investigate the Safety and Effectiveness of the Technolas® TENEO 317 Model 2 Excimer Laser for Laser In Situ Keratomileusis (LASIK) Surgery to Treat Myopia or Myopic Astigmatism

Study identification

NCT ID
NCT04111757
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bausch & Lomb Incorporated
Industry
Enrollment
168 participants

Conditions and interventions

Interventions

  • Technolas® TENEO 317 Model 2 Device

Device

Eligibility (public fields only)

Age range
22 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
Jul 24, 2019
Primary completion
Aug 5, 2021
Completion
Aug 5, 2021
Last update posted
Jun 13, 2024

2019 – 2021

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Bausch Site 101 Newport Beach California 92663
Bausch Site 110 Blaine Minnesota 55434
Bausch Site 107 Bloomington Minnesota 55420
Bausch Site 108 Omaha Nebraska 68105
Bausch Site 106 Portsmouth New Hampshire 03801
Bausch Site 102 Amherst New York 14228
Bausch Site 104 Greensboro North Carolina 27401
Bausch Site 103 Mt. Pleasant South Carolina 29464
Bausch Site 109 Sioux Falls South Dakota 57108
Bausch Site 105 Cedar Park Texas 78613

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 NCT04111757, 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 Jun 13, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04111757 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →