[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"myopia-moderate\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:myopia-moderate":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100580638","a-prospective-randomized-clinical-study-of-two-phakic-toric-implantable-lenses-100580638",false,"NCT06839898","A Prospective, Randomized Clinical Study of Two Phakic Toric Implantable Lenses","A Prospective, Randomized Clinical Study of Two Phakic Toric Implantable Lenses to Compare Outcomes in Patients With Moderate to High Myopia and Astigmatism","Inclusion Criteria:\n\n* Patients 21 years old or older.\n* Calculated IOL Power is within the range of the investigational IOLs\n* Corneal Cylindrical error within the range defined in the clinical investigation plan\n* Subject has monocular UCVA 0.5 LogMAR or worse\n* Subject has had a stable refraction (±0.5D; ±1.0D for higher refractive errors), as expressed by manifest refraction spherical equivalent (MRSE) for a minimum 12 months prior to surgery, verified by consecutive refractions and\u002For medical records or prescription history.\n* Subject, who is a current contact lens wearer, needs to demonstrate a stable refraction (±0.5D) expressed as MRSE, on two consecutive examination dates and stability of the refraction is determined by the following criteria:\n\n  1. Contact lenses were not worn for at least 2 weeks or 3 days prior to the first refraction.\n  2. Two refractions were performed at least 7 days apart.\n* Subject, who is expected to have residual postoperative cylindrical refractive error of ≥1D, has been given the opportunity to experience his\u002Fher best spectacle vision with the anticipated correction.\n* Expected dilated pupil size at least large enough to visualize the axis marking.\n* Patients willing to attend all follow-up appointments\n* Patients must sign and be given a copy of the written Informed Consent form\n\nExclusion Criteria:\n\n* Subject with acute and chronic disease or illness that would increase the operative risk or confound the outcomes of the evaluation.\n* Subject taking systematic medication that can confound the outcome of the study or increase the risk to the subject\n* Subject with ocular condition that may predispose the subject to future complications\n* Subject with previous intraocular or corneal surgery\n* Subject with less than the minimum endothelial cell density 2000 cells\u002Fmm² at the time of enrollment\n* Pregnant or planning to become pregnant, or is lactating during the course of the evaluation\n* Other condition associated with fluctuation of hormones\n* ACD measured from the endothelium lower than 2.8 mm\n* Concurrent participation in another drug or device evaluation.\n* Any cataract of any grade.\n* Coefficient of variation of endothelial cell area \\>0.45\n* Percent Hexagonality of endothelial cell shape ≤ 45%\n* Monocular subject\n* Vulnerable subjects as defined in section 12.3.10","ALL","21 Years",{"count":19,"type":20},172,"ESTIMATED","INTERVENTIONAL",[23],"NA","Primary Objective: To compare the efficacy and the residual refractive error of EYECRYLTM Phakic toric versus Visian® Toric ICL in moderate to high myopic patient with co-existing astigmatism. Secondary Objectives: To evaluate and compare the safety of EYECRYLTM Phakic toric versus Visian® Toric ICL in moderate to high myopic patients with co-existing astigmatism.",[26,27,28],"Myopia, Moderate","Myopic Astigmatism","Myopia, Degenerative","RECRUITING","2025-02-17",{"date":32,"type":33},"2025-02-21","ACTUAL",{"date":35,"type":33},"2021-10-10",{"date":37,"type":20},"2027-02",{"name":39,"class":40},"Biotech Healthcare Holding Gmbh","INDUSTRY",4,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100520665","software-refraction-with-mobilerone-versus-retinoscopy-100520665","NCT06059521","Software Refraction With Mobilerone Versus Retinoscopy","Randomized Controlled Study on Subjective Refraction by Software Eye Test Technology Versus Retinoscopy","SRMR","Inclusion Criteria:\n\n* • subject with ametropia on each eye ≤-12.00D\n\n  * subject with best corrected visual acuity ≥ 20\u002F25, no amblyopia\n  * subject with normal transparency of eyes\n  * subject with a healthy fundus that does not reveal major abnormalities that may affect vision due to the fluctuate situations\n  * subject able to cooperate with the screen and the operator\n  * subject without heavy drug treatment that may affect vision as synthetic antimalarials, corticosteroids\n  * non-diabetic subject\n  * non nystagmus subject\n  * non-strabismus subject\n  * subject who has not had eye surgery less than 1 year old\n\nExclusion Criteria:\n\n* • subject with a topography showing an anomaly (keratoconus type or other)\n\n  * subject with hyperopia or presbyopia\n  * subject with mild myopia ≥ -1.00D\n  * subject who cannot speak with the operator including those staff of local optometrists or ophthalmologists",true,"10 Years","46 Years",{"count":54,"type":20},120,[23],"Software refraction in the mobilerone for myopia and astigmatism is a novel medical device for myopia adults and elder children with or without astigmatism. And the investigators would like to test its accuracy and efficacy as well as safety.",[58,26,59],"Myopia","Astigmatism",[61,62,63,64,65,66],"software","refraction","subjective refraction","mobilerone","myopia","astigmatism","2023-09-21",{"date":69,"type":33},"2023-09-28",{"date":71,"type":33},"2023-07-15",{"date":73,"type":20},"2030-12-30",{"name":75,"class":40},"Beijing Airdoc Technology Co., Ltd.",3]