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Multifocal Lenses

Multifocal Contact Lenses for Presbyopia

N/A
Recruiting
Led By Jennifer Fogt, OD, MS
Research Sponsored by Jennifer Fogt
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
At least 38 years of age or older
Previously dropped out of contact lens wear due to vision or vision and discomfort
Must not have
Current or active ocular inflammation or infection as determined by the Investigator
History of previous eye surgery
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 month
Awards & highlights
No Placebo-Only Group

Summary

This trial is to see if presbyopic adults who have stopped using contact lenses can use Dailies TOTAL1 Multifocal contact lenses.

Who is the study for?
This trial is for adults over 38 who used to wear contact lenses but stopped due to vision issues or discomfort. They must have good general health, stable medication use, and a corrected visual acuity of 20/25 or better. People with eye inflammation/infection, high astigmatism, binocular vision problems, pregnancy/lactation, past eye surgery or corneal conditions can't join.
What is being tested?
The study tests Dailies TOTAL1 Multifocal soft contact lenses in presbyopic individuals who previously quit using contacts. Participants will evaluate their experience over three required visits with potential additional follow-ups.
What are the potential side effects?
While the trial primarily assesses comfort and vision quality with multifocal lenses, potential side effects may include eye irritation or dryness, blurred vision during adjustment period and less commonly allergic reactions.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 38 years old or older.
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I stopped using contact lenses because they were uncomfortable or affected my vision.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I do not have any eye infections or inflammation.
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I have had eye surgery in the past.
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I have a history of corneal ectasia or keratoconus.

Timeline

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

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Quality of Life Survey
Visual Analog Scale

Awards & Highlights

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

Trial Design

1Treatment groups
Experimental Treatment
Group I: Lens wear experienceExperimental Treatment1 Intervention
Subject will wear contact lenses for about a month during the day.

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Who is running the clinical trial?

Alcon ResearchIndustry Sponsor
731 Previous Clinical Trials
128,879 Total Patients Enrolled
37 Trials studying Presbyopia
6,500 Patients Enrolled for Presbyopia
Jennifer FogtLead Sponsor
2 Previous Clinical Trials
52 Total Patients Enrolled
Jennifer Fogt, OD, MSPrincipal InvestigatorOhio State University
3 Previous Clinical Trials
75 Total Patients Enrolled
~14 spots leftby Nov 2025
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