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Wear Experience With Daily Disposable Contact Lenses for Astigmatism Over a Long-Wear Day

Wear Experience With Daily Disposable Contact Lenses for Astigmatism Over a Long-Wear Day

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07303920
Enrollment
40
Registered
2025-12-26
Start date
2026-03-04
Completion date
2026-06-30
Last updated
2026-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Astigmatism

Brief summary

The purpose of this study to assess the wear experience of people who have astigmatism when wearing a daily disposable contact lens for astigmatism over long days of wear.

Interventions

DEVICEDaily disposable contact lenses for astigmatism

All participants will be fit with the study lenses

Sponsors

Ohio State University
Lead SponsorOTHER
Alcon Research
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Current soft toric contact lens wearer with long hours of wear * Willing to follow the contact lens wearing schedule required by the study * Vision 20/25 or better with current soft toric contact lenses * Self-report completion of a comprehensive eye examination in the past two years

Exclusion criteria

* Have a history of corneal ocular surgery * Have current ocular inflammation or infection as assessed by the study investigator who will complete the study * Are past rigid contact lens wearers * Have a history of being diagnosed with dry eye or ocular allergies * Have known systemic health conditions that are thought to alter tear film physiology * Have a history of viral eye disease * Have a history of ocular surgery * Have a history of severe ocular trauma * Have a history of corneal dystrophies or degenerations * Have active ocular infection or inflammation * Are currently using isotretinoin-derivatives or ocular medications * Are pregnant or breast feeding

Design outcomes

Primary

MeasureTime frameDescription
ComfortMeasured over 16 hours of wearProportion of participants with positive Visual Analog Scale (VAS, \>50 on a 0-100 scale)

Countries

United States

Contacts

CONTACTStudy Coordinators
OPT-EyeStudies@osu.edu614-292-8858

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026