ClinicalTrials.Veeva

Menu

Evaluation of Wear Experience With One Week Reusable Contact Lenses in Habitual Two Week Reusable Lens Wearers

The Ohio State University logo

The Ohio State University

Status

Completed

Conditions

Myopia

Treatments

Device: One week replacement contact lenses
Device: Biweekly replacement contact lenses

Study type

Interventional

Funder types

Other

Identifiers

NCT06382064
2024H0089

Details and patient eligibility

About

This open-label study is of current Acuvue® Oasys® wearers (2 - week replacement, reusable lenses) who are satisfied with their current lenses. Subjects will be refit into one week reusable contact lenses and will wear lenses for approximately 2 weeks. Subjects will return for vision and lens fit assessments and will complete surveys about their wear experience.

Enrollment

71 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. At least 18 years of age
  2. Ability to give informed consent
  3. Current Acuvue® Oasys® spherical lens wearer.
  4. Distance visual acuity of 20/25 or better with current contact lenses in each eye.
  5. Good general health defined by, medication use that has not changed within the last 30 days and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the Investigator.
  6. Willing to spend time for the study, which includes: attend three study visits and wear contact lenses on days between study visits.

Exclusion criteria

  1. Current or active ocular inflammation or infection as determined by the Investigator.
  2. Currently pregnant or lactating. (Participants will be asked to self-report these conditions).
  3. Systemic inflammatory disease (i.e. Diabetes, etc.) that could confound study results in the opinion of the investigator.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

71 participants in 1 patient group

Contact Lens Wear Experience
Experimental group
Description:
Participants will be enrolled in the study for 4 weeks. Biweekly replacement contact lenses will be worn for the first 2 weeks. One-week replacement lenses worn for second 2 weeks.
Treatment:
Device: Biweekly replacement contact lenses
Device: One week replacement contact lenses

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems