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NCT06382064

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

Evaluation of Wear Experience With PRECISION7® Contact Lenses in Habitual Acuvue® Oasys® Lens Wearers
Ohio State University·ClinicalTrials.gov·device·Device trialRecruitment Completed
View on ClinicalTrials.gov →
Study focus
Disease/Condition
Myopia
Drug/Device/Intervention
Biweekly replacement contact lenses
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Ohio State University
Location
Columbus, United States of America
Timeline & enrollment
Phase
N/A
Start date
Apr 16, 2024
End date
May 01, 2025
Enrollment
80 participants
Primary outcome

Subjective assessment of lens wear experience

Summary

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.

ICD-10 classifications
MyopiaDegenerative myopiaAmblyopia ex anopsiaOcular myiasisMyiasis
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06382064
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06382064 through Pure Global AI's free database. This phase not specified trial is sponsored by Ohio State University and is currently Recruitment Completed. The study focuses on Myopia. Target enrollment is 80 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.