Soft peripheral contact lens for eye elongation control (SPACE): 1-year results of a double-blinded randomized controlled trial.
Autor: | Lee SC; Department of Medical Imaging And Radiological Sciences, Chung Shan Medical University, Taichung, Taiwan., Hsu MY; Department of Ophthalmology, Chung Shan Medical University Hospital, Taichung, Taiwan; School of Medicine, Chung Shan Medical University, Taichung, Taiwan., Huang SC; Department of Nutrition, Chung Shan Medical University, Taichung, Taiwan., Chen C; Department of Optometry, Chung Shan Medical University, Taichung, Taiwan; Institute of Optometry, Chung Shan Medical University, Taichung, Taiwan. Electronic address: cconnie7@csmu.edu.tw. |
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Jazyk: | angličtina |
Zdroj: | Contact lens & anterior eye : the journal of the British Contact Lens Association [Cont Lens Anterior Eye] 2024 Oct; Vol. 47 (5), pp. 102256. Date of Electronic Publication: 2024 Jul 03. |
DOI: | 10.1016/j.clae.2024.102256 |
Abstrakt: | Purpose: To examine the safety and efficacy of soft multifocal contact lenses on slowing the rate of myopia progression. Methods: A prospective, randomized, double-masked clinical trial was conducted including 115 children (55 boys and 60 girls) aged 8 to 15 years. Children were assigned to wear one of two daily disposable soft contact lens designs; a multifocal design (Pegavision) or a dual-focus design (MiSight, Coopervision) in both eyes for at least 8 h per day for one year. All contact lenses were replaced on a daily basis. Measurements were obtained using a logMAR vision meter, including objective refraction, handheld retinoscopy, high (96 %) and low (12 %) contrast sensitivity, and distance and near visual acuity. Axial length was measured every 6 months. Results: After one year, the spherical equivalent refractive error and axial length of the experimental group (Pegavision) increased by -0.50 ± 0.48 D and 0.24 ± 0.16 mm, respectively, in the right eye and -0.47 ± 0.37 D and 0.23 ± 0.16 mm, respectively, in the left eye. The spherical equivalent refractive error and axial length of the control group (MiSight) increased by -0.48 ± 0.47 D and 0.22 ± 0.13 mm, respectively, in the right eye and by -0.50 ± 0.44 D and 0.23 ± 0.14 mm, respectively, in the left eye, with no significant differences observed between the two lens types. Conclusions: The one-year results from this clinical trial show that the multifocal soft contact lenses used in the experimental group have a similar myopia control efficacy with respect to spherical equivalent refraction and axial length elongation as a commercially available dual focus soft contact lens design. (Copyright © 2024. Published by Elsevier Ltd.) |
Databáze: | MEDLINE |
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