NCT06616480

A Study to Evaluate the Safety and Efficacy of DSFNC1 Soft Hydrophilic Contact Lenses and SiHy Color Soft Hydrophilic Contact Lenses

Multicenter, Open, Parallel, Randomized Controlled Comparison on the Safety and Efficacy Clinical Study of DSFNC1 Soft Hydrophilic Contact Lenses With SiHy Color Soft Hydrophilic Contact Lenses

• 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 DSFNC1 soft hydrophilic contact lenses with SiHy color soft hydrophilic contact lenses.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	BenQ Materials DSFNC1 soft hydrophilic contact lenses	Test lenses were to be worn for approximately 90 days.
DEVICE	Visco SiHy Color soft hydrophilic contact lenses	Control lenses were to be worn for approximately 90 days

Timeline

• Start date: 2023-03-03
• Primary completion: 2024-03-28
• Completion: 2024-06-20
• First posted: 2024-09-27
• Last updated: 2024-09-27

Locations

1 site across 1 country: China