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Evaluation of Wear Experience With One Week Reusable Contact Lenses in Habitual Two Week Reusable Lens Wearers - Trial NCT06382064

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.

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Trial Details
ClinicalTrials.gov โ€ข NCT06382064
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Evaluation of Wear Experience With One Week Reusable Contact Lenses in Habitual Two Week Reusable Lens Wearers
Evaluation of Wear Experience With PRECISION7ยฎ Contact Lenses in Habitual Acuvueยฎ Oasysยฎ Lens Wearers

Study Focus

Myopia

Biweekly replacement contact lenses

Interventional

device

Sponsor & Location

Ohio State University

Columbus, United States of America

Timeline & Enrollment

N/A

Apr 16, 2024

May 01, 2025

80 participants

Primary Outcome

Subjective assessment of lens wear experience

Summary

This open-label study is of current Acuvueยฎ Oasysยฎ 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

Myopia
Degenerative myopia
Amblyopia ex anopsia
Ocular myiasis
Myiasis

Data Source

ClinicalTrials.gov

NCT06382064

Device Trial