Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05102383
Other study ID # 2021H0305
Secondary ID
Status Completed
Phase N/A
First received
Last updated
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
Health authority
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

Study Design


Related Conditions & MeSH terms


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
See also
  Status Clinical Trial Phase
Completed NCT04535310 - Wear Experience With Daily Contact Lenses Over a Long Day N/A
Completed NCT05416528 - Chinese Translation and Validation of the 8-item Contact Lens Dry Eye Questionnaire (CLDEQ-8)
Completed NCT05096156 - Evaluation of Wear Experience With Daily Contact Lenses N/A
Completed NCT04844281 - Wear Experience With Daily Toric Contact Lenses Over a Long Day N/A
Recruiting NCT02713399 - High-resolution Imaging of Tear Film Thickness in Contact Lenses Wearers With Optical Coherence Tomography (OCT). A Pilot Study
Completed NCT04296877 - Evaluation of Wear Experience With a Daily Disposable Contact Lens N/A
Completed NCT06335212 - Peripheral Defocus Profile of Multifocal Minus Contact Lenses
Completed NCT03686878 - Lifitegrast 5% Ophthalmic Solution and Contact Lens Dryness Phase 4