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Short-Term Clinical Comparison of Two Silicone Hydrogel Daily Disposable Contact Lenses

NCT03139578 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2019-02-01

Study results available
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Summary

This will be a 2 period one-day, double-masked, randomized, repeated measures, non-dispensing, cross-over study where the main purpose of this study is to compare the performance of a new daily disposable silicone hydrogel lens with that of an existing similar lens.

Conditions

  • Visual Acuity

Interventions

DEVICE

Test 8.5BC

senofilcon A contact lenses with 8.5 base curve

DEVICE

Test 9.0BC

senofilcon A contact lenses with 9.0 base curve

DEVICE

Control 8.5BC

narafilcon A contact lenses with 8.5 base curve

DEVICE

Control 9.0BC

narafilcon A contact lenses with 9.0 base curve

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-04-28
Primary Completion
2017-10-22
Completion
2017-10-22
FDA Device
Yes

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 NCT03139578 on ClinicalTrials.gov