NCT04709237

Evaluation of The Clinical Acceptance of Soft Contact Lenses for Myopia Control

• Status: Completed
• Phase: —
• Study type: Interventional
• Enrollment: 21 (actual)
• Sponsor: CooperVision, Inc. · Industry
• Sex: All
• Age: 10 Years – 16 Years
• Healthy volunteers: Accepted

Summary

The main objective of the study was to evaluate the clinical acceptance of soft contact lenses for Myopia control.

Detailed description

Participants were randomized to wear each study contact lenses for 10 days with investigator and participant masking. The participants who are not contact lens wearer at enrollment wore single vision contact lenses for two weeks during the pre-investigation phase to get adapted to contact lens wear.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	omafilcon A control lens	Participants were randomized to wear omafilcon A control soft contact lens for 10 days.
DEVICE	omafilcon A test lens 1	Participants were randomized to wear omafilcon A test soft contact lens 1 for 10 days.
DEVICE	omafilcon A test lens 2	Participants were randomized to wear omafilcon A test soft contact lens 2 for 10 days.

Timeline

• Start date: 2019-12-14
• Primary completion: 2021-03-31
• Completion: 2021-03-31
• First posted: 2021-01-14
• Last updated: 2024-08-27
• Results posted: 2024-08-27

Locations

1 site across 1 country: United Kingdom