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Contact Lens

Evaluation of Etafilcon A Daily Disposable Lenses

N/A
Waitlist Available
Research Sponsored by Johnson & Johnson Vision Care, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1-week follow-up
Awards & highlights
No Placebo-Only Group

Summary

To evaluate the clinical performance of daily disposable etafilcon A lenses.

Eligible Conditions
  • Near-sightedness

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1-week follow-up
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1-week follow-up for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Monocular Logarithm of the Minimum Angle of Resolution (logMAR) Visual Acuity - Standard High Contrast Dim
Monocular logMar Visual Acuity - Standard Low Contrast Bright
Overall Comfort
+1 more

Side effects data

From 2014 Phase 1 & 2 trial • 289 Patients • NCT01437319
10%
Cornea Lens Peripheral Ulcer (CLPU)
10%
Conjunctivitis
5%
Asymptomatic corneal scar
100%
80%
60%
40%
20%
0%
Study treatment Arm
Comfilcon A
Balafilcon A
Lotrafilcon A

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Etafilcon A Test LensExperimental Treatment1 Intervention
etafilcon A
Group II: Etafilcon A Control LensActive Control1 Intervention
etafilcon A
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
etafilcon A
2008
Completed Phase 2
~2620

Find a Location

Who is running the clinical trial?

Johnson & Johnson Vision Care, Inc.Lead Sponsor
219 Previous Clinical Trials
25,655 Total Patients Enrolled
~11 spots leftby Jan 2026