NCT06616519

A Study to Evaluate the Safety and Efficacy of MSENC1 Soft Hydrophilic Contact Lenses and Oxypure Color Soft Hydrophilic Contact Lenses

Multi-center, Open, Parallel, and Randomly Controlled Comparison Between MSENC1 Soft Hydrophilic Contact Lenses and Oxypure Color Soft Hydrophilic Contact Lenses in Their Safety and Efficacy

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 192 (actual)
• Sponsor: BenQ Materials Corporation · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This project is an open, parallel, randomly controlled, and non-inferiority clinical trial of MSENCI soft hydrophilic contact lenses with Oxypure color soft hydrophilic contact lenses used as the control product.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	BenQ Materials MSENCI soft hydrophilic contact lenses	Test lenses were to be worn for approximately 90 days.
DEVICE	Visco Oxypure Color soft hydrophilic contact lenses	Control lenses were to be worn for approximately 90 days

Timeline

• Start date: 2021-05-18
• Primary completion: 2022-05-01
• Completion: 2022-08-25
• First posted: 2024-09-27
• Last updated: 2024-09-27

Locations

1 site across 1 country: China