[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Myoptechs, Inc\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":63},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,39],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":4},"100631207","evaluation-of-novel-spectacles-intended-for-myopia-management-in-a-short-term-study-100631207",false,"NCT07497672","Evaluation of Novel Spectacles Intended for Myopia Management in a Short-Term Study","Inclusion Criteria:\n\n1. 8 - 15 years of age, inclusive.\n2. Ability of the child to assent, and for one parent to provide permission to participate.\n3. Had an eye examination within the past year.\n4. Distance visual acuity of 20\u002F25 (logMAR +0.10) or better in each eye with best corrected with sph\u002Fcyl subjective refraction.\n5. Habitual glasses wearer of either MiYOSMART or Stellest for at least 2 months. (Can also be a contact lens wearer but needs to wear either MiYOSMART or Stellest spectacles for a minimum of 6 hours on a typical day.)\n6. No history of binocular function anomaly (e.g., no history of strabismus), and no apparent strabismus.\n7. Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data, as determined by the investigator).\n\nExclusion Criteria:\n\n1. Current report of active ocular inflammation or infection.\n2. Astigmatism \\> 1.00 D in either eye\n3. History of previous eye surgery","ALL","8 Years","15 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","The primary objective of this study is to evaluate the visual acuity, wearability, and quality of vision with two novel multifocal glasses designs in habitual myopia control glasses wearers, in a non-dispensing study after short-term wear.",[26],"Myopia: Refractive Error","NOT_YET_RECRUITING","2026-03-26",{"date":30,"type":31},"2026-04-01","ACTUAL",{"date":33,"type":20},"2026-04-15",{"date":35,"type":20},"2026-12-15",{"name":37,"class":38},"Myoptechs, Inc","INDUSTRY",{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":44,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":15,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":49,"briefSummary":50,"conditions":51,"keywords":4,"overallStatus":53,"whyStopped":4,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":62},"100604902","measuring-changes-in-choroidal-thickness-induced-by-prototype-soft-contact-lenses-worn-for-1-hour-100604902","NCT07155551","Measuring Changes In Choroidal Thickness Induced By Prototype Soft Contact Lenses Worn For 1 Hour","ARCTIC","Inclusion Criteria:\n\n* Are 18-25 years of age (inclusive) and have full legal capacity to volunteer; Have read (or be read to) and signed the information and consent form; Habitually wear soft contact lenses or are spectacle wearers with previous experience of soft contact lens wear;\n* Are myopic with both eyes having a vertex corrected spherical equivalent non-cycloplegic refraction of at least -0.50 DS and no more than -4.50 DS;\n* Achieve at least LogMAR +0.10 with spherical equivalent refraction in each eye;\n* Are willing and able to maintain the appointment schedule and follow the measurement visit instructions which include no use of caffeine drinks, alcohol or other stimulants 12 hours before each measurement visit and no smoking or use of recreational cannabis 24 hours before the study visit;\n* Have not used a myopia control treatment within 2 years prior to Visit 0 (this includes multifocal spectacle or contact lens wear, orthokeratology, or atropine);\n* Typically sleeps at least 7 hours per night.\n\nExclusion Criteria:\n\n* Participating in any concurrent clinical or research study;\n* Have astigmatism of more than 1.00 DC in either eye as per non-cycloplegic refraction;\n* Have amblyopia in either eye or known to have any other binocular vision disorder, such as accommodative insufficiency;\n* Have any known active\\* ocular disease and\u002For infection;\n* Have a systemic condition that in the opinion of the investigator may affect a study outcome variable. Examples include diabetes mellitus, hyperthyroidism, and active allergies;\n* Are using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable. Examples include antihistamine, atropine eye drops;\n* Have known sensitivity to the sodium fluorescein diagnostic pharmaceutical to be used in the study;\n* Self-reports as pregnant, lactating or planning a pregnancy at the time of enrolment;\n* Have undergone strabismus surgery, refractive error surgery or intraocular surgery;\n* Are an employee of the Centre for Ocular Research \\& Education directly involved in this study (i.e. on the delegation log).","18 Years","25 Years",{"count":19,"type":20},[23],"The objective of the study is to evaluate the short-term change in choroidal thickness induced by 3 prototype soft contact lenses for people with myopia.",[52],"Myopia; Refractive Error","RECRUITING","2025-08-27",{"date":56,"type":31},"2025-09-04",{"date":58,"type":20},"2025-08-25",{"date":60,"type":20},"2025-12",{"name":37,"class":38},1,""]