Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Oct 21, 2026, 1:20 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 31, 2018 (Actual)
Primary completion
May 4, 2023 (Actual)
Completion
May 4, 2023 (Actual)
Last update posted
Dec 24, 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 24, 2024 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03603600 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →