Clinical Trials Directory

Trials / Completed

CompletedNCT03681808

Evaluate the Safety and Effectiveness of the Biotrue ONEday for Astigmatism

A Study to Evaluate the Safety and Effectiveness of the Biotrue ONEday for Astigmatism Soft Contact Lens When Worn on a Daily Basis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
242 (actual)
Sponsor
Bausch & Lomb Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Comparing Test Lens for Astigmatism Soft Contact Lens (Test) to 1-Day Control for Astigmatism contact lenses (Control).

Detailed description

This is a multicenter, randomized 1:1, parallel-group, bilateral, Investigator-masked study at 13 investigative sites in the United States (US) in a population including Chinese subjects (maternal and paternal grandparents born in China)

Conditions

Interventions

TypeNameDescription
DEVICEControlContact Lens
DEVICETestSoft Contact Lens

Timeline

Start date
2018-10-10
Primary completion
2019-12-16
Completion
2019-12-16
First posted
2018-09-24
Last updated
2021-01-08
Results posted
2020-12-17

Locations

13 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03681808. Inclusion in this directory is not an endorsement.

Evaluate the Safety and Effectiveness of the Biotrue ONEday for Astigmatism (NCT03681808) · Clinical Trials Directory