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Clinical Comparison of Silicone Hydrogel Monthly Lenses

NCT03169153 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2019-07-25

Study results available
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Summary

The purpose of this study is to compare AIR OPTIX® plus HydraGlyde (AOHG) contact lenses to ACUVUE® VITA® (VITA) contact lenses for total lipid uptake (total of surface and bulk uptake) after 30 days of wear by high lipid depositors.

Conditions

  • Refractive Error

Interventions

DEVICE

Lotrafilcon B contact lenses

Silicone hydrogel contact lenses used as per their Conformité Européenne (CE) marking

DEVICE

Senofilcon C contact lenses

Silicone hydrogel contact lenses used as per their Conformité Européenne (CE) marking

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Manager, Medical Clinical Trial Services · 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
2017-09-22
Primary Completion
2018-07-19
Completion
2018-07-19

Countries

  • United Kingdom

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 NCT03169153 on ClinicalTrials.gov