The A.R.R.E.S.T.® Contact Lens Study

Launched by NTHALMIC PTY LTD · Mar 13, 2025

Keywords

ClinConnect Summary

The A.R.R.E.S.T.® Contact Lens Study is a clinical trial designed to find out if special contact lenses using a new technology called A.R.R.E.S.T.® can help slow down the worsening of myopia (nearsightedness) in children. The main questions the study aims to answer are whether these lenses can reduce the growth of the eye (which contributes to worsening vision) and whether they can help keep myopia from getting worse as quickly as regular single vision contact lenses.

Children between the ages of 7 and 15 who are myopic may be eligible to participate. To join, they need to have a parent or guardian who can understand and agree to the study. Participants will be randomly assigned to wear either the A.R.R.E.S.T.® contact lenses or regular contact lenses and will need to visit the clinic seven times over a year. They must also commit to wearing the study lenses for at least 6 hours a day, five days a week. It's important to note that the study is not yet recruiting participants, and there are specific health requirements that must be met to ensure safety during the research.

Gender

ALL

Eligibility criteria

• • Inclusion Criteria
• • Be between 7 to 15 years old inclusive at time of enrolment.
• * Have:
• • Read the Informed Assent.
• • Been explained the Informed Assent.
• • Indicated an understanding of the Informed Assent.
• • Signed the Informed Assent.
• • Have their parent / legal guardian.
• • Read the Informed Consent.
• • Been explained the Informed Consent.
• • Indicated an understanding of the Informed Consent.
• • Signed the Informed Consent.
• • Along with their parent/legal guardian, be capable of comprehending the nature of the study and be willing to adhere to the study requirements.
• • Along with their parent/legal guardian, agree to maintain the visit and prescribed wearing schedule.
• • Agree to wear the study contact lenses for a minimum of 5 days/week, 6 hours/day 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.
• • Be in good general health, based on parent's/legal guardian's knowledge.
• • Have best-corrected high contrast visual acuity of 0.10 logMAR (Snellen: 20/25, 6/7.6; Decimal: 0.80) or better in each eye.
• * Meet the following criteria determined by cycloplegic autorefraction at Baseline:
• • -4.00 D ≤ spherical equivalent ≤ 0.75 D
• • -1.00 DC ≤ astigmatic component ≤ 0 DC
• • Participants who fail astigmatism criterion with autorefraction pass astigmatism criterion if ≥ 0.75 D is measured with subjective refraction.
• • \|Spherical equivalent anisometropia\| ≤ 1.00 D.
• • Exclusion Criteria
• • Participant in another study within 30 days prior to this study.
• * Current or prior use of interventions intended for myopia control, including but not limited to:
• * Optical devices:
• • Bifocal / multifocal spectacles.
• • Bifocal / multifocal contact lenses.
• • Orthokeratology.
• * Pharmacological agents:
• • Atropine with a concentration \> 0.01%.
• • 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.
• • Pirenzepine.
• • Participant born earlier than 30 weeks or weighed \< 1500 g at birth.
• • o A verbal report from the participant's parent / legal guardian is sufficient.
• • Habitual use of a systemic or topical medication that may alter normal ocular findings / is known to affect a participant's ocular health / physiology either in an adverse or beneficial manner at enrolment and / or during the clinical trial.
• • A known allergy to sodium fluorescein, benoxinate, proparacaine, tropicamide, or cyclopentolate.
• • A known corneal hypoesthesia (reduced corneal sensitivity), corneal ulcer, corneal infiltrates, ocular viral or fungal infections, or any other recurrent ocular infections.
• • Strabismus as determined by cover test at distance (≥ 3 m) or near (40 cm) while wearing distance correction under non-cycloplegic conditions.
• * Known ocular or systemic disease, such as but not limited to:
• • Diabetes.
• • Graves' disease.
• • Glaucoma.
• • Uveitis.
• • Scleritis.
• • Auto immune diseases such as ankylosing spondylitis, multiple sclerosis, Sjogrens syndrome, and systemic lupus erythematosus.
• * Any ocular, systemic, or neuro-developmental conditions that could influence refractive development, such as but not limited to:
• • Persistent pupillary membrane.
• • Vitreous haemorrhage.
• • Cataract.
• • Central corneal scarring.
• • Eyelid haemangiomas.
• • Marfan's syndrome.
• • Down's syndrome.
• • Ehler's-Danlos syndrome.
• • Stickler's syndrome.
• • Ocular albinism.
• • Retinopathy of prematurity.
• • Keratoconus or irregular cornea.
• * Biomicroscopic that contraindicate contact lens, such as but not limited to:
• • Neovascularisation or ghost vessels ≥ 1.5 mm in from limbus.
• • Any active anterior segment disease that contraindicates safe contact lens wear.
• • Clinically significant giant papillary conjunctivitis.
• • Clinically significant abnormalities of the anterior segment, lids, conjunctiva, sclera, or associated structures.
• • Allergic or seasonal conjunctivitis if the investigator believes it could significantly interfere with maintaining a specified wearing schedule.
• • 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.