NCT04116736

ACUVUE® OASYS With Transitions™ Light Intelligent Technology™ Clinical Performance Registry

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 146 (actual)
• Sponsor: Johnson & Johnson Vision Care, Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

This registry study is a one-year, one-visit, observational, prospective, open-label, two-arm, multi-center, multi-national, post-market study of approximately 300 patients who have recently been fitted with the ACUVUE® OASYS with Transitions™ and approximately 300 patients who have recently been fitted with spherical nonphotochromic reusable marketed silicone hydrogel contact lenses (of any brand). Eligible subjects will be asked to complete a Patient Registration Questionnaire several times throughout the year.

Conditions

• Vision Satisfaction in Bright Light

Interventions

Type	Name	Description
DEVICE	ACUVUE® OASYS with Transitions™	JJVC Marketed Contact Lens
DEVICE	Silicone Hydrogel Contact Lens	Any reusable spherical silicone hydrogel brand that is approved and marketed in the country conducting the study.

Timeline

• Start date: 2019-10-19
• Primary completion: 2023-03-10
• Completion: 2023-03-10
• First posted: 2019-10-07
• Last updated: 2025-05-23
• Results posted: 2025-05-23

Locations

22 sites across 2 countries: Spain, United Kingdom

Regulatory

• FDA-regulated device study