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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05495971
Other study ID # VTI-2206
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 6, 2022
Est. completion date May 12, 2023

Study information

Verified date May 2024
Source Visioneering Technologies, Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

VTI has an FDA cleared soft contact lens product. Its optical design creates an enhanced depth of focus (EDOF), which provides clear distance, intermediate, and near vision. This study is to quantify the enhanced depth of focus and visual impact.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date May 12, 2023
Est. primary completion date May 12, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 70 Years
Eligibility Inclusion Criteria: - Suitable and able to wear contact lenses - Normal best corrected vision (20/25 or better) - Need reading add +2.00 or stronger Exclusion Criteria: - Pre-existing ocular condition that would contraindicating lens wear

Study Design


Related Conditions & MeSH terms


Intervention

Device:
NaturalVue Multifocal
EDOF

Locations

Country Name City State
United States VTI Alpharetta Georgia

Sponsors (1)

Lead Sponsor Collaborator
Visioneering Technologies, Inc

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary LogMAR Visual Acuity Vision at different viewing conditions 4 hours
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