Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
ID07586982

Clinical Performance of Verofilcon A Toric Contact Lenses in Satisfied Wearers of Senofilcon A Toric Contact Lenses With Blue Light Filtration

Led by Southern College of Optometry · Updated on 2026-05-14

32

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the comfort, vision, and satisfaction of the TOTAL30 Multifocal Toric contact lenses in adults who have previously worn reusable silicone hydrogel toric contact lenses and are now presbyopic. The study focuses on presbyopic adults aged 18 to 40 who have astigmatism and are transitioning to these new contact lenses. The trial aims to determine whether these lenses provide good visual acuity, comfort, and willingness to continue use after one month of wear. Participants will be refit with the TOTAL30 Multifocal Toric contact lenses, which are monthly silicone hydrogel lenses designed to provide comfort throughout the day. The study involves wearing the lenses daily for at least 13 hours, without overnight use, and includes assessments at Day 1, Day 14, and Day 29 via text message to track comfort and vision. The study is prospective and focuses on those currently using reusable silicone hydrogel toric lenses, with astigmatism between 0.75 and 2.50 diopters in each eye. During the study, participants will undergo evaluations including visual acuity testing and completion of the Contact Lens Dry Eye 8 questionnaire to measure comfort levels. Researchers will collect comfort ratings on Days 1, 14, and 29 and monitor how well participants adapt to the lenses. The main outcome is visual acuity after one month of wear, along with comfort and dryness scores. The total participation period includes one month of lens wear and monitoring, with the study ending in September 2026.

CONDITIONS

Brief Title

Clinical Performance of Verofilcon A Toric Contact Lenses

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 40 years
  • Current or recent reusable silicone hydrogel toric contact lens wearers with best-corrected 20/20 distance vision or better
  • Require +0.75 ADD or more for near vision at 40 cm
  • Astigmatism between 0.75 and 2.50 diopters in each eye
  • Contact Lens Dry Eye 8 questionnaire score less than 12
  • Able to wear Total30 Multifocal Toric lenses daily for at least 13 hours without overnight use
  • Willing to wear lenses every day and complete comfort assessments on Days 1, 14, and 29
  • Provide a glasses prescription less than 3 years old
  • Visual acuity of 20/25 or better with habitual reusable toric lenses in each eye
Not Eligible

You will not qualify if you...

  • Previous use of Total30 Multifocal Toric lenses
  • Past rigid contact lens wearers
  • Current use of monovision contact lenses
  • History of dry eye or ocular allergies
  • Systemic health conditions affecting tear film
  • History of viral eye disease
  • History of ocular surgery or severe eye trauma
  • Corneal dystrophies or degenerations
  • Active eye infection or inflammation
  • Current use of isotretinoin derivatives or ocular medications
  • Pregnant or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - 1 month

Participants are refit into Total30 Multifocal Toric contact lenses and wear them daily.

1 baseline visit and assessments via text messages on Days 1, 14, and 29

Trial Site Locations

Total: 1 location

1

The Southern College of Optometry

Memphis, Tennessee, United States, 38104

Actively Recruiting

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Research Team

C

Chris Lievens, OD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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