AzTrials
AzTrials

AstigmatismNCT07303920

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

A study testing Daily disposable contact lenses for astigmatism in people with Astigmatism, run by Ohio State University at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

Search all trials

Trial 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. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Astigmatism
What is being tested?
Daily disposable contact lenses for astigmatism
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteUnited States
Study dates
4 Mar 2026to 30 Dec 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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
Show all 12Show fewer
  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Study Coordinators contact

614-292-8858

OPT-EyeStudies@osu.edu

United States1 site, 1 recruiting
  • The Ohio State University College of Optometry

    Columbus, Ohio, 43210

    Emma Grant, 614-292-8858, OPT-EyeStudies@osu.edu

    Emily Wagner, 614-292-8858, OPT-EyeStudies@osu.edu

    Recruiting

Other trials in United States

About this study

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.

Conditions
Astigmatism
Being tested
Daily disposable contact lenses for astigmatism
Medical subject headings
Astigmatism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Daily disposable contact lenses for astigmatismDevice

    Also called Dailies Total1 for Astigmatism

    All participants will be fit with the study lenses

Study groups in NCT07303920
Study groupRoleWhat they receive
Contact Lens WearOtherAll participants will be fit with the study contact lenses for astigmatism
Receives: Device: Daily disposable contact lenses for astigmatism

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Comfort

    Proportion of participants with positive Visual Analog Scale (VAS, >50 on a 0-100 scale)

    Measured: Measured over 16 hours of wear

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Dec 2025
  2. Study start4 Mar 2026
  3. Primary completion30 Dec 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07303920
Sponsor's protocol ID
20252462
Status last verified
Sep 2026
First submitted
23 Dec 2025
Last updated
25 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in