The Effectiveness and Acceptability of Dual-focus Soft Contact Lenses for Controlling Rapid Progressive Myopia in Young Adults: A Randomized Controlled Trial
| Registry | NCT06528860 |
|---|---|
| Status | Not yet recruiting |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: triple, treatment |
| Enrollment | 144 (Estimated) |
| Sponsor | Shanghai Eye Disease Prevention and Treatment Center (Other) |
| Conditions | Myopia |
| Interventions | MiSight® 1 day soft contact lenses, Proclear® 1 day soft contact lenses (Device) |
| Dates | start 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 |
| Locations | 1 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
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.
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.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Dual-focus CL | Experimental | Device: MiSight® 1 day soft contact lenses | Wearing dual-focus CL for 2 years |
| Single-vision CL | Placebo comparator | Device: Proclear® 1 day soft contact lenses | Wearing single-vision CL for 2 years |
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.
| Facility | City | Country | Status |
|---|---|---|---|
| Shanghai Eye Disease Prevention & Treatment Center | Shanghai, Shanghai Municipality | China |