Dual-focus Soft Contact Lenses for Controlling Rapid Progressive Myopia in Young Adults

NCT06528860 — Not applicable, Not yet recruiting, 144 participants, Shanghai Eye Disease Prevention and Treatment Center

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The Effectiveness and Acceptability of Dual-focus Soft Contact Lenses for Controlling Rapid Progressive Myopia in Young Adults: A Randomized Controlled Trial

RegistryNCT06528860
StatusNot yet recruiting
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: triple, treatment
Enrollment144 (Estimated)
SponsorShanghai Eye Disease Prevention and Treatment Center (Other)
ConditionsMyopia
InterventionsMiSight® 1 day soft contact lenses, Proclear® 1 day soft contact lenses (Device)
Datesstart 2024-08-31 (estimated), primary completion 2027-06-30 (estimated), completion 2027-09-30 (estimated), first posted 2024-07-30, last updated 2024-07-30
Locations1 site in China

Related Papers Related Patents Related Grants Related Experts
All trials for Myopia All trials of MiSight® 1 day soft contact lenses All trials of Proclear® 1 day soft contact lenses

-Summary

This study aims to evaluate the effectiveness and acceptability of dual-focus soft contact lenses in controlling rapid myopia progression in adults through a randomized controlled trial. By applying myopia control measures to the adult population, we hope to provide scientific evidence for the effective control of adult myopia progression and offer insights into the understanding of myopia progression during early adulthood.

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+Detailed description

It has long been believed that the progression of myopia mainly occurs during the elementary to high school stages. However, some studies and clinical practice suggest that a considerable proportion of adults still experience myopia progression in their adulthood, especially in those who have prolonged near work or screen usage time. At present, there is insufficient evidence on whether these population needs myopia control intervention. Most adults experiencing myopia progression do not receive appropriate myopic intervention measures, leading to an increase of dioptre, which may affect the quality of daily life, and raise the risk of high myopia and blinding myopia complications.

This study aims to evaluate the effectiveness and acceptability of dual-focus soft contact lenses in controlling rapid myopia progression in adults through a randomized controlled trial. By applying myopia control measures to the adult population, we hope to provide scientific evidence for the effective control of adult myopia progression and offer insights into the understanding of myopia progression during early adulthood.

+Arms and interventions

ArmTypeInterventionsDescription
Dual-focus CLExperimentalDevice: MiSight® 1 day soft contact lensesWearing dual-focus CL for 2 years
Single-vision CLPlacebo comparatorDevice: Proclear® 1 day soft contact lensesWearing single-vision CL for 2 years
  • MiSight® 1 day soft contact lenses (Device), also known as CooperVision: Dual-focus contact lenses, daily disposable, material: omafilcon A, water content: 60%.
  • Proclear® 1 day soft contact lenses (Device), also known as CooperVision: Single-vision contact lenses, daily disposable, material: omafilcon A, water content: 60%.

+Outcome measures

Primary outcomes

  • Change in cycloplegic spherical equivalent after 2 years [2 years after the baseline]: The difference in the change of cycloplegic spherical equivalent between the intervention group and the control group.

Secondary outcomes

  • Change in axial length after 2 years [2 years after the baseline]: The difference in the change of axial length between the intervention group and the control group.

+Eligibility

Sex: All, ages: 18 Years to 25 Years

Inclusion Criteria:

* Age 18-25 years;
* Myopia progression <= -0.50D in either eye in the past year (evaluated by -manifest refraction);
* The subject eye: cycloplegic spherical equivalent ranges from -2.00D to -6.0D and cylinder power doesn't exceed -1.50D;
* The subject eye's best corrected visual acuity <= logMAR 0.1;
* Anisometropia does not exceed 1.50D.

Exclusion Criteria:

* Current use of MC interventions or prior use of MC interventions within the past 6 months;
* Disease or anatomical factors that affect the wearing of contact lenses;
* History of myopia correction surgery;
* Suffering from ocular or systemic diseases that may be related to myopia, such as Marfan syndrome, retinopathy of prematurity, diabetes, etc.;
* pregnant female;
* Other conditions deemed unsuitable by the investigators.

+Locations (1)

FacilityCityCountryStatus
Shanghai Eye Disease Prevention & Treatment CenterShanghai, Shanghai MunicipalityChina

+Publications

  • Ruiz-Pomeda A, Villa-Collar C. Slowing the Progression of Myopia in Children with the MiSight Contact Lens: A Narrative Review of the Evidence. Ophthalmol Ther. 2020 Dec;9(4):783-795. doi: 10.1007/s40123-020-00298-y. Epub 2020 Sep 11. PMID 32915454
  • Bullimore MA, Lee SS, Schmid KL, Rozema JJ, Leveziel N, Mallen EAH, Jacobsen N, Iribarren R, Verkicharla PK, Polling JR, Chamberlain P. IMI-Onset and Progression of Myopia in Young Adults. Invest Ophthalmol Vis Sci. 2023 May 1;64(6):2. doi: 10.1167/iovs.64.6.2. PMID 37126362

+Investigators

  • Xiangui He, Principal investigator, Shanghai Eye Disease Prevention & Treatment Center