Management of Myopia in University Students Using Dual Focus Soft Contact Lenses (MoMUS)

University of Bradford

Status: Invitation-only

Conditions: Myopia, Progressive

Treatments: Device: MiSight contact lenses; Device: Proclear contact lenses

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05955638

E1060

Details and patient eligibility

About

The purpose of the study is to quantify the effectiveness of Coopervision MiSight contact lenses in slowing the rate of myopia progression in university students.

Full description

MiSight contact lenses have been shown to be a safe and effective way of managing myopia progression in children aged 8-12 years. However, myopic progression is not limited to children of this age group and MiSight lenses have also been shown to be effective in older children aged 11-16 years. There is evidence that progression also occurs in university students. The researchers are therefore investigating the effectiveness of this intervention in a group of UK-based University students.

Enrollment: 84 estimated patients

Sex: All

Ages: 18 to 21 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Be a myopic students studying at university
• Be aged 18-21 years at the start of the study
• Show evidence of recent myopia progression prior to commencement of Stage 2 of the study.
• Have read the patient information sheet and be happy to sign the consent forms
• Be willing to adhere to the visit schedule and wearing times described in this protocol
• Agree to lens wearing times of at least 10 hours per day, 6 days per week
• Agree to accept either the control or test lens as assigned by the randomisation
• Have BCVA of +0.10 logMAR or better in each eye

Exclusion criteria

• Previous myopia control use (optical or pharmacological)
• Amblyopia
• Ocular pathology such as keratoconus or recurrent corneal infections
• Myopic Rx > 10D
• Astigmatism >1D
• Anisometropia >1.75D
• Binocular Vision anomalies (such as Tropia)
• Medications that affect pupil size or accommodation
• A known allergy to fluorescein or tropicamide
• Biomicroscopic findings that would contraindicate contact lens wear
• The investigator considers that it is not in the best interest of the subject to participate in the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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84 participants in 2 patient groups

MiSight dual focus contact lens

Experimental group

Treatment:

Device: MiSight contact lenses

Proclear single vision contact lens

Active Comparator group

Treatment:

Device: Proclear contact lenses