MedPath

Spectacle Films Utilising S.T.O.P.® Technology for Slowing Down Myopia Progression in Children

Not Applicable
Recruiting
Conditions
Myopia
Interventions
Device: Standard single vision spectacle lens + S.T.O.P.® Kit 1 or 2
Device: Single vision spectacle lens + S.T.O.P.® Kit 1
Device: Single vision spectacle lens
Device: Single vision spectacle lens + S.T.O.P.® Kit 2
Device: Single vision spectacle lens + S.T.O.P.® Film
Registration Number
NCT06137560
Lead Sponsor
nthalmic Pty Ltd
Brief Summary

There are two parts to this trial. First, to compare the rate of myopia progression of spectacle films using Spatio Temporal Optic Phase (S.T.O.P.®) technology that provide a dynamic optical cue against single vision spectacle lenses. Second, to compare the rate of myopia progression of spectacle films using S.T.O.P.® technology that provide a dynamic optical cue against spectacle films using S.T.O.P.® technology that provide a static optical cue. A dynamic optical cue is one that changes, and a static optical cue is one that does not change.

Detailed Description

In the first part of the trial, myopic children (6-14 years of age) will be randomly allocated to wear one of three spectacle lens options (standard single vision spectacle lenses, standard single vision spectacle lenses + S.T.O.P.® Kit 1 spectacle films, or standard single vision spectacle lenses + S.T.O.P.® Kit 2 spectacle films). S.T.O.P.® spectacle films are applied to the front surface of standard single vision spectacle lenses. Both S.T.O.P.® Kits 1 and 2 are comprised of two different sets of spectacle films applied to two different pairs of single vision spectacle lenses which are worn on alternate weeks, and thus both S.T.O.P.® Kits 1 and 2 provide a dynamic optical cue.

In the second part of this trial, participants will be randomly allocated wear of of two spectacle lens options (the best performer from S.T.O.P.® Kits 1 and 2 in terms of reducing the rate of myopic progression and single vision spectacle lenses + S.T.O.P.® film). As previously stated, both S.T.O.P.® Kits 1 and 2 provide a dynamic optical cue while S.T.O.P.® film provide a static optical cue.

The overall trial duration, including follow-up period, is expected to be approximately 42 months. Each participant's duration is expected to be approximately 30 months.

The visits are Baseline, Dispensing, 1 month, 4 months, 6 months, then visits every 6 months after.

All procedures performed at these visits are standard, non invasive clinical tests.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
210
Inclusion Criteria
  • Be between 6-14 years 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 and able to adhere to study requirements.

  • Along with their parent / legal guardian, agree to maintain the visit and prescribed wearing schedule.

  • Agree to wear allocated spectacles for a minimum of 5 days per week, at least 6 hours per day for the duration of the study and to inform the investigator if their schedule is interrupted.

  • Possess wearable and visually functioning spectacles.

  • Be in good general health, based on the parent's / legal guardian's knowledge.

  • Have best-corrected high contrast visual acuity based on manifest refraction of 0.10 logMAR (20/25, 6/7.6) or better in each eye.

  • Meet the following criteria determined by cycloplegic autorefraction at Baseline:

    • -5.00 D ≤ spherical equivalent ≤ -0.75 D and sphere component ≤ -0.50 DS.
    • -1.50 DC ≤ astigmatic component ≤ 0 DC.
    • |Spherical equivalent anisometropia| ≤ 1.00 D.
Exclusion Criteria
  • Participant is currently, or within 30 days prior to this study, has been an active participant in another study.

  • Current or prior use of ANY form of myopia control, including but not limited to:

    • Optical devices:

      • Bifocal or multifocal spectacles of any type.
      • Bifocal or multifocal contact lenses of any type.
      • Orthokeratology of any type.
    • 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.

    • 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.

  • 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.

  • 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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Assigned Intervention 5Standard single vision spectacle lens + S.T.O.P.® Kit 1 or 2Dynamic optical signal: single vision spectacle lens + S.T.O.P.® Kit 1 or 2
Assigned Intervention 2Single vision spectacle lens + S.T.O.P.® Kit 1Single vision spectacle lens + S.T.O.P.® Kit 1
Assigned Intervention 1Single vision spectacle lensSingle vision spectacle lens
Assigned Intervention 3Single vision spectacle lens + S.T.O.P.® Kit 2Single vision spectacle lens + S.T.O.P.® Kit 2
Assigned Intervention 4Single vision spectacle lens + S.T.O.P.® FilmStatic optical signal: single vision spectacle lens + S.T.O.P.® spectacle film
Primary Outcome Measures
NameTimeMethod
Axial lengthSecond Dispense (up to 392 days from Baseline), then 6 months, 12 months, and 18 months after Second Dispense

Difference in change from Second Dispense in axial length between static optical cue (control) and dynamic optical cue (test)

Secondary Outcome Measures
NameTimeMethod
Visual performance as measured by high contrast visual acuity at 6 m6 months, 12 months, and 18 months after Second Dispense (up to 392 days from Baseline)

Difference in visual performance between static optical cue (control) and dynamic optical cue (test)

Visual performance as measured by a non validated questionnaire based on a 1-106 months, 12 months, and 18 months after Second Dispense (up to 26 days from Baseline)

Difference in visual performance between static optical cue (control) and dynamic optical cue (test)

Cycloplegic spherical equivalent autorefractionSecond Dispense (up to 392 days from Baseline), then 6 months, 12 months, and 18 months after Second Dispense

Difference in change from Second Dispense in cycloplegic spherical equivalent autorefraction between static optical cue (control) and dynamic optical cue (test)

Trial Locations

Locations (5)

Tianjin Eye Hospital

🇨🇳

Tianjin, Heping District, China

Shanghai Fudan University Eye and ENT Hospital

🇨🇳

Shanghai, Xuhui District, China

Divyajyoti Trust Tejas Eye Hospital

🇮🇳

Surat, Gujarat, India

LV Prasad Eye Institute

🇮🇳

Hyderabad, Telangana, India

Pristine Eye Hospitals

🇮🇳

Hyderabad, Telangana, India

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