Wear Experience With Daily Disposable Contact Lenses for Astigmatism Over a Long-Wear Day
NCT ID: NCT07303920
Last Updated: 2025-12-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
40 participants
INTERVENTIONAL
2026-01-15
2026-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
OTHER
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Contact Lens Wear
All participants will be fit with the study contact lenses for astigmatism
Daily disposable contact lenses for astigmatism
All participants will be fit with the study lenses
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Daily disposable contact lenses for astigmatism
All participants will be fit with the study lenses
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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 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
18 Years
40 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Alcon Research
INDUSTRY
Ohio State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jennifer Fogt
Assistant Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The Ohio State University College of Optometry
Columbus, Ohio, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Emma Grant
Role: primary
Emily Wagner
Role: backup
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20252462
Identifier Type: -
Identifier Source: org_study_id