Performance and Safety of Silicone Hydrogel Soft Contact Lenses
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Myopia
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Participant)Primary Purpose: Treatment
Participation Requirements
- Age
- Between 20 years and 45 years
- Gender
- Both males and females
Description
This study is a prospective, subject-masked, bilateral, randomized, parallel group dispensing study comparing the SHSCL test lens against the 1-Month ACUVUE® VITA™ (1-MAV) control lenses. Each subject will be randomized to wear either the test or of the control with similar/comparable lens parameter...
This study is a prospective, subject-masked, bilateral, randomized, parallel group dispensing study comparing the SHSCL test lens against the 1-Month ACUVUE® VITA™ (1-MAV) control lenses. Each subject will be randomized to wear either the test or of the control with similar/comparable lens parameters optimized for vision. Both test and control lens will be used in their daily wear, monthly replacement modality for thirteen (13) weeks. It is anticipated that this study will involve up to 6 scheduled visits.
Tracking Information
- NCT #
- NCT04226560
- Collaborators
- Chang Gung Memorial Hospital
- Taipei Medical University WanFang Hospital
- Investigators
- Principal Investigator: Yih-Shiou Hwang, M.D.,Ph.D. Chang Gung Memorial Hospital Principal Investigator: Hsin-Wei Huang, M.D. Taipei Medical University - Municipal Wan Fang Hospital
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