Evaluation of Wear Experience With a Water Surface Daily Disposable Contact Lens

Contact Lens Clinical Trial

Official title:

Evaluation of Wear Experience With a Water Surface Daily Disposable Contact Lens

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05102383
• Other study ID #: 2021H0305
• Status: Completed
• Phase: N/A
• Start date: November 15, 2021
• Est. completion date: April 19, 2022

Study information

• Verified date: November 2023
• Source: Ohio State University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the wear experience of existing wearers of a monthly replacement contact lens after they have been fit with a daily disposable contact lens that has water surface treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 34
• Est. completion date: April 19, 2022
• Est. primary completion date: April 19, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Must be a current wearer of Comfilcon A contact lenses

• Distance visual acuity of 20/25 or better with current contact lenses

• Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the PI)

• Ability to give informed consent

• Willing to spend time for the study, which includes attending three study visits and be willing to wear contact lenses on days between study visits.

• Either gender.

• Any racial or ethnic origin.

Exclusion Criteria:

• No current ocular inflammation or infection.

• Not currently pregnant or lactating

Related Conditions & MeSH terms

• Contact Lens

Intervention

Device:
• Comfilcon A Toric contact lenses
Monthly replacement contact lenses
• Verofilcon A for Astigmatism Daily Disposable contact lenses
Daily disposable contact lenses

Locations

Country	Name	City	State
United States	The Ohio State University College of Optometry	Columbus	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Subjective Assessment of Overall Comfort With Verofilcon A Daily Disposable Lenses for Astigmatism	Participants will complete a Visual Analog Scale survey of overall comfort (0-100 Scale with 0 anchored with "Poor Comfort" and 100 anchored as "Excellent Comfort")	3 weeks