Presbyopia Clinical Trials

Find Presbyopia Clinical Trials Near You

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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to \[primary purpose: is to determine if Total30 Multi focal toric conntact lensesare comfortable and the willigness for those who have previously worn reusable toric contact lenses are willing to stay in Total30 MFT after 1 month of wear during the duration of the study. Healthy previous reusable toric contact lens weareres will be refit into total30 MFT contact lenses and will be asked to gauge their comfort while wearing the lenses. Healthy adult participants who are presybyopic between the ages of 18-40 can participant, sex and gender are not disqualifiers unless the participant is pregnant or breast feeding. The main question\[s\] it aims to answer \[is/are\] \[primary hypothesis or outcome measure 1Proportions of toric CL wearers who have positive visual acuity scores in comfort and vision after one month of wear. \[primary hypothesis or outcome measure 2\]? Contact lens dry eye-8 scores will be less than 12 indicating high levels of comfort after one month of wear.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 40
Healthy Volunteers: t
View:

• Adults, ≥40-year-old, CL wearers with best-corrected 20/20 distance visual acuity or better.

• Requiring +0.75 ADD or more at standard near distance of 40 cm.

• Participants will be required to have worn reusable silicone hydrogel toric CLs in the past year and still at a minimum wearing the CLs occasionally without having significant discomfort or dryness.

• All participants will be required to have a CLDEQ-8 score \<12.

• Participants will be required to be able to wear Total 30MFT CLs (presbyopic plus astigmatism both ≥0.75D OD and OS).

• Astigmatism ranging from 0.75 D to 2.50 D in each eye.

• Participants will be required to wear the study CLs for ≥13 hours each day with no overnight wear.

• Willing to wear study CLs for ≥16 hours on the Day 1 (1st full day), Day 14, and Day 29 when responses will be collected via text message.

• Participants will be willing to wear the CL every day of the week.

• Participants will be required to provide a glasses prescription that is less than 3 years old.

• Visual acuity with habitual reusable silicone hydrogel toric CLs is 20/25 or better in each eye.

Locations
United States
Tennessee
The Southern College of Optometry
RECRUITING
Memphis
Contact Information
Primary
Chris Lievens, OD
clievens@sco.edu
(901) 722-3200
Time Frame
Start Date: 2026-04
Estimated Completion Date: 2026-09
Participants
Target number of participants: 32
Treatments
Experimental: TOTAL30 Multifocal Toric contact lenses
This will be a prospective study to understand if reusable silicone hydrogel toric CL wearers who are presbyopic can be successfully refit into Total30 MFT CLs
Related Therapeutic Areas
Sponsors
Leads: Southern College of Optometry

This content was sourced from clinicaltrials.gov