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Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 1

NCT04527978 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2021-11-23

Study results available
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Summary

The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to Biotrue ONEday contact lenses.

Conditions

  • Refractive Errors
  • Myopia

Interventions

DEVICE

Verofilcon A contact lenses

Spherical soft contact lenses for daily disposable wear

DEVICE

Nesofilcon A contact lenses

Spherical soft contact lenses for daily disposable wear

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • CDMA Project Lead, Vision Care · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-15
Primary Completion
2020-11-06
Completion
2020-11-06
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04527978 on ClinicalTrials.gov