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Completed Not applicable Interventional Results available

A Study of B + L Ophthalmic Viscosurgical Device (OVD) CVisc50

ClinicalTrials.gov ID: NCT04192630

Public ClinicalTrials.gov record NCT04192630. 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 3, 2026, 8:19 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

A Study to Document the Safety and Effectiveness of a New Cohesive OVD When Compared to a Control OVD

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 Bausch \& Lomb CVisc50 cohesive OVD compared to the Alcon ProVisc® cohesive OVD when used in cataract surgery.

Study identification

NCT ID
NCT04192630
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bausch & Lomb Incorporated
Industry
Enrollment
390 participants

Conditions and interventions

Conditions

Interventions

Device · Procedure

Eligibility (public fields only)

Age range
45 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
Nov 25, 2019
Primary completion
Jan 30, 2022
Completion
Jan 30, 2022
Last update posted
May 27, 2024

2019 – 2022

United States locations

U.S. sites
22
U.S. states
10
U.S. cities
21
Facility City State ZIP Site status
Bausch Site 017 Chandler Arizona 85224
Bausch Site 001 Phoenix Arizona 85032
Bausch Site 008 Fayetteville Arkansas 72704
Bausch Site 010 Burlingame California 94010
Bausch Site 007 Garden Grove California 92843
Bausch Site 011 Newport Beach California 92662
Bausch Site 012 Northridge California 91325
Bausch Site 013 Rancho Cordova California 95670
Bausch Site 004 Torrance California 90505
Bausch Site 019 Bloomington Minnesota 55420
Bausch Site 020 Kansas City Missouri 64154
Bausch Site 002 St Louis Missouri 63131
Bausch Site 015 Washington Missouri 63090
Bausch Site 005 New York New York 10013
Bausch Site 021 Mason Ohio 45040
Bausch Site 003 Reading Pennsylvania 96002
Bausch Site 014 Goodlettsville Tennessee 37073
Bausch 018 Nashville Tennessee 37215
Bausch Site 009 Cedar Park Texas 78613
Bausch Site 006 Houston Texas 77008
Bausch 022 San Antonio Texas 78215
Bausch Site 016 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 NCT04192630, 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 May 27, 2024 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04192630 live on ClinicalTrials.gov.

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