[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"nthalmic Pty Ltd\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":44},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100583576","the-arrest-contact-lens-study-100583576",false,"NCT06878118","The A.R.R.E.S.T.® Contact Lens Study","Prospective, Controlled, Randomised, Contralateral Wear, Dispensing Trial to Assess the Efficacy of Contact Lenses Using A.R.R.E.S.T.® Technology","Inclusion Criteria\n\n* Be between 7 to 15 years old inclusive at time of enrolment.\n* Have:\n\n  * Read the Informed Assent.\n  * Been explained the Informed Assent.\n  * Indicated an understanding of the Informed Assent.\n  * Signed the Informed Assent.\n* Have their parent \u002F legal guardian.\n\n  * Read the Informed Consent.\n  * Been explained the Informed Consent.\n  * Indicated an understanding of the Informed Consent.\n  * Signed the Informed Consent.\n* Along with their parent\u002Flegal guardian, be capable of comprehending the nature of the study and be willing to adhere to the study requirements.\n* Along with their parent\u002Flegal guardian, agree to maintain the visit and prescribed wearing schedule.\n* Agree to wear the study contact lenses for a minimum of 5 days\u002Fweek, 6 hours\u002Fday on days lenses are worn but not \\> 16 hours per day, and to remove lenses at night (i.e., daily wear only with no contact lens wear during sleep), for the duration of the study and to inform the investigator if their schedule is interrupted. Wearing time can be modified by the investigator for health reasons.\n* Be in good general health, based on parent's\u002Flegal guardian's knowledge.\n* Have best-corrected high contrast visual acuity of 0.10 logMAR (Snellen: 20\u002F25, 6\u002F7.6; Decimal: 0.80) or better in each eye.\n* Meet the following criteria determined by cycloplegic autorefraction at Baseline:\n\n  * -4.00 D ≤ spherical equivalent ≤ 0.75 D\n  * -1.00 DC ≤ astigmatic component ≤ 0 DC\n* Participants who fail astigmatism criterion with autorefraction pass astigmatism criterion if ≥ 0.75 D is measured with subjective refraction.\n\n  * \\|Spherical equivalent anisometropia\\| ≤ 1.00 D.\n\nExclusion Criteria\n\n* Participant in another study within 30 days prior to this study.\n* Current or prior use of interventions intended for myopia control, including but not limited to:\n* Optical devices:\n\n  * Bifocal \u002F multifocal spectacles.\n  * Bifocal \u002F multifocal contact lenses.\n  * Orthokeratology.\n* Pharmacological agents:\n\n  * Atropine with a concentration \\> 0.01%.\n  * Participants who have previously used 0.01% atropine are eligible for this study provided they agree not to use 0.01% atropine for at least 30 days before baseline and at any time during the study.\n  * Pirenzepine.\n* Participant born earlier than 30 weeks or weighed \\\u003C 1500 g at birth.\n\n  o A verbal report from the participant's parent \u002F legal guardian is sufficient.\n* Habitual use of a systemic or topical medication that may alter normal ocular findings \u002F is known to affect a participant's ocular health \u002F physiology either in an adverse or beneficial manner at enrolment and \u002F or during the clinical trial.\n* A known allergy to sodium fluorescein, benoxinate, proparacaine, tropicamide, or cyclopentolate.\n* A known corneal hypoesthesia (reduced corneal sensitivity), corneal ulcer, corneal infiltrates, ocular viral or fungal infections, or any other recurrent ocular infections.\n* Strabismus as determined by cover test at distance (≥ 3 m) or near (40 cm) while wearing distance correction under non-cycloplegic conditions.\n* Known ocular or systemic disease, such as but not limited to:\n\n  * Diabetes.\n  * Graves' disease.\n  * Glaucoma.\n  * Uveitis.\n  * Scleritis.\n  * Auto immune diseases such as ankylosing spondylitis, multiple sclerosis, Sjogrens syndrome, and systemic lupus erythematosus.\n  * Any ocular, systemic, or neuro-developmental conditions that could influence refractive development, such as but not limited to:\n  * Persistent pupillary membrane.\n  * Vitreous haemorrhage.\n  * Cataract.\n  * Central corneal scarring.\n  * Eyelid haemangiomas.\n  * Marfan's syndrome.\n  * Down's syndrome.\n  * Ehler's-Danlos syndrome.\n  * Stickler's syndrome.\n  * Ocular albinism.\n  * Retinopathy of prematurity.\n  * Keratoconus or irregular cornea.\n* Biomicroscopic that contraindicate contact lens, such as but not limited to:\n\n  * Neovascularisation or ghost vessels ≥ 1.5 mm in from limbus.\n  * Any active anterior segment disease that contraindicates safe contact lens wear.\n  * Clinically significant giant papillary conjunctivitis.\n  * Clinically significant abnormalities of the anterior segment, lids, conjunctiva, sclera, or associated structures.\n  * Allergic or seasonal conjunctivitis if the investigator believes it could significantly interfere with maintaining a specified wearing schedule.\n* The investigator may, at their discretion, exclude anyone who they believe may not be able to fulfil the clinical trial requirements or it is believed to be in the participant's best interests.","ALL","7 Years","15 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn if contact lenses using Active Reconfiguration in Retinal Encoding of Spatio-Temporal (A.R.R.E.S.T.®) signal technology works to slow down the rate of myopia progression compared to single vision contact lenses in myopic children. The main questions it aims to answer are:\n\nDo contact lenses using A.R.R.E.S.T.® technology slow down the rate of axial length growth? Do contact lenses using A.R.R.E.S.T.® technology slow down the rate of increase in myopic refractive error?\n\nResearchers will compare contact lenses using A.R.R.E.S.T.® technology to a single vision contact lens.\n\nParticipants will:\n\nBe randomly allocated to wear either contact lenses using A.R.R.E.S.T.® technology or single vision contact lenses.\n\nVisit the clinic on seven occasions over a 12 month period.",[27,28],"Myopia","Myopia Progression",[30],"axial length","RECRUITING","2025-09-29",{"date":34,"type":35},"2025-10-03","ACTUAL",{"date":37,"type":35},"2025-07-06",{"date":39,"type":21},"2026-11-01",{"name":41,"class":42},"nthalmic Pty Ltd","NETWORK",2,""]