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Food and Drug Administration, American Academy of Ophthalmology, American Academy of Optometry, American Association for Pediatric Ophthalmology and Strabismus, American Optometric Association, American Society of Cataract and Refractive Surgery, and Contact Lens Association of Ophthalmologists Co-Sponsored Workshop: Controlling the Progression of Myopia: Contact Lenses and Future Medical Devices.
Walline, Jeffrey J; Robboy, Marc W; Hilmantel, Gene; Tarver, Michelle E; Afshari, Natalie A; Dhaliwal, Deepinder K; Morse, Christie L; Quinn, Christopher J; Repka, Michael X; Eydelman, Malvina B.
Afiliação
  • Walline JJ; College of Optometry (J.J.W.), The Ohio State University, Columbus, OH; Office of Device Evaluation (M.W.R., G.N.H., M.E.T., M.B.E.), Center for Devices and Radiological Health, Food and Drug Administration, Silver Spring, MD; Division of Cornea and Refractive Surgery (N.A.A.), Shiley Eye Institute, La Jolla, CA; Refractive Surgery and the Cornea Service (D.K.D.), University of Pittsburgh Medical Center Eye Center, Pittsburgh, PA; Concord Eye Center (C.L.M.), Concord, NH; Omni Eye Services (C.J.
Eye Contact Lens ; 44(4): 205-211, 2018 Jul.
Article em En | MEDLINE | ID: mdl-29923881
ABSTRACT
The prevalence of myopia is high and increasing. Approximately 5 billion people around the world are expected to be myopic by the year 2050. Methods to slow the progression of myopia and therefore potentially decrease the associated sight-threatening complications have been the subject of a number of investigations. A workshop, sponsored by the United States Food and Drug Administration (FDA) Center for Devices and Radiological Health, American Academy of Ophthalmology, American Academy of Optometry, American Association for Pediatric Ophthalmology and Strabismus, American Optometric Association, American Society of Cataract and Refractive Surgery, and Contact Lens Association of Ophthalmologists, Inc, convened myopia experts from around the world to discuss principles to consider in the design of clinical trials investigating the effectiveness and safety of myopia control devices. Experts discussed parameters such as study endpoints, duration, enrollment criteria, patient-reported outcomes, recruitment, and retention. The discussions among the experts, FDA, and audience members should help to facilitate the development and evaluation of reasonably safe and effective myopia control devices.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dispositivos Ópticos / Miopia Tipo de estudo: Guideline / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dispositivos Ópticos / Miopia Tipo de estudo: Guideline / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article