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Completed Not applicable Interventional Accepts healthy volunteers Results available

Evaluate the Safety and Effectiveness of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens

ClinicalTrials.gov ID: NCT03603600

Public ClinicalTrials.gov record NCT03603600. 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 Sep 2, 2026, 8:06 AM 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 Prospective, Multicenter, Randomized, Active-Controlled Clinical Study to Evaluate the Safety and Effectiveness of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens in Subjects Undergoing Cataract Extraction

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of the study is to evaluate the safety and effectiveness of the enVista trifocal intraocular lens when implanted in the capsular bag.

Study identification

NCT ID
NCT03603600
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bausch & Lomb Incorporated
Industry
Enrollment
501 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
22 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
May 30, 2018
Primary completion
May 3, 2023
Completion
May 3, 2023
Last update posted
Dec 23, 2024

2018 – 2023

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Bausch Site 108 Fayetteville Arkansas 72703
Bausch Site 113 Garden Grove California 02843
Bausch Site 120 Northridge California 91325
Bausch Site 115 Redding California 96002
Bausch Site 103 Torrance California 90505
Bausch Site 107 Mt. Dora Florida 32757
Bausch Site 117 Lake Villa Illinois 60046
Bausch Site 101 Bloomington Minnesota 55420
Bausch Site 119 Birmingham Mississippi 49009
Bausch Site 102 St Louis Missouri 63131
Bausch Site 124 Omaha Nebraska 68137
Bausch Site 118 Las Vegas Nevada 89145
Bausch Site 106 Brecksville Ohio 44141
Bausch Site 109 Columbus Ohio 43215
Bausch Site 116 Pittsburgh Pennsylvania 16066
Bausch Site 121 Sioux Falls South Dakota 57108
Bausch Site 112 Memphis Tennessee 38119
Bausch Site 110 Nashville Tennessee 37205
Bausch Site 104 Cedar Park Texas 78613
Bausch Site 105 Dallas Texas 75243
Bausch Site 111 Houston Texas 77008
Bausch Site 122 San Antonio Texas 78215
Bausch Site 123 San Antonio Texas 78229

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 NCT03603600, 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 Dec 23, 2024 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03603600 live on ClinicalTrials.gov.

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