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Clinical Performance of a Silicone Hydrogel Contact Lens Following One Night of Extended Wear

NCT03560141 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2021-07-28

Study results available
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Summary

The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens following 1 night of extended wear.

Conditions

  • Refractive Errors

Interventions

DEVICE

LID011121 contact lens

Investigational silicone hydrogel contact lens

DEVICE

Comfilcon A contact lens

Commercially available silicone hydrogel contact lens

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
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-11
Primary Completion
2018-07-17
Completion
2018-07-17
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 NCT03560141 on ClinicalTrials.gov