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Performance Assessment of a Modified Daily Disposable Contact Lens

NCT03762668 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2020-01-13

Study results available
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Summary

The purpose of this study is to compare visual acuity between two daily disposable contact lenses.

Conditions

  • Refractive Errors
  • Myopia
  • Hyperopia

Interventions

DEVICE

Modified delefilcon A contact lenses

Spherical soft daily disposable contact lens

DEVICE

Delefilcon A contact lenses

Spherical soft daily disposable contact lens

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Sr. CDMA Project Lead, Vision Care · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-03
Primary Completion
2019-01-07
Completion
2019-01-07
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 NCT03762668 on ClinicalTrials.gov