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Assessment of an Investigational Frequent Replacement Silicone Hydrogel Lens

NCT04085328 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 675

Last updated 2023-06-13

Study results available
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Summary

The purpose of this clinical trial is to evaluate the safety and performance of an investigational soft contact lens compared to a commercially available soft contact lens when worn in an extended wear modality.

Conditions

  • Refractive Ametropia

Interventions

DEVICE

LID015385 soft contact lenses

Investigational silicone hydrogel contact lenses for up to 6 nights/7 days of continuous wear

DEVICE

Comfilcon A soft contact lenses

Silicone hydrogel contact lenses for up to 6 nights/7 days of continuous wear

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Alcon Study Director · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-11
Primary Completion
2021-03-26
Completion
2021-03-26
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 NCT04085328 on ClinicalTrials.gov