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Atropine Alone vs Atropine Plus Bifocal Spectacles for Myopia Control in Children (COMBAT-Myopia)

20 maggio 2026 aggiornato da: Dr Memoona Arshad, University of Faisalabad

Investigating Comparative Efficacy of Myopia Control Strategies and Genetic Underpinnings: A Randomized Controlled Trial

Background: Myopia (nearsightedness) is a growing global health concern, projected to affect 50% of the world population by 2050. Children with progressive myopia are at risk of serious ocular complications including myopic maculopathy, glaucoma, and retinal detachment. Low-dose atropine (0.05%) has shown efficacy in slowing myopia progression, and optical interventions such as bifocal spectacles may provide additional benefits by altering peripheral retinal defocus. Objective: This randomized controlled trial aims to compare the efficacy and effectiveness of atropine 0.05% monotherapy versus combination therapy (atropine 0.05% plus bifocal spectacles) in controlling myopia progression in children. Methods: Children aged 4-16 years with bilateral myopia (cycloplegic spherical equivalent between -1.00 D and -6.00 D) and documented recent progression (≥ -0.50 D in the preceding 12 months) will be randomized 1:1 to receive either atropine 0.05% eye drops once daily or atropine 0.05% plus bifocal spectacles. The primary outcome is change in spherical equivalent refraction over 12 months; the secondary outcome is change in axial length. Follow-up visits occur at 3, 6, 9, and 12 months. Conclusion: This study will provide evidence on whether adding bifocal correction to pharmacological therapy offers superior myopia control compared to atropine alone, informing clinical practice guidelines for pediatric myopia management.

Panoramica dello studio

Descrizione dettagliata

Study Design and Setting:

This is a prospective, randomized, parallel-group, controlled trial conducted at the Department of Ophthalmology, Mayo Hospital, Lahore, Pakistan. The study is designed and reported in accordance with CONSORT (Consolidated Standards of Reporting Trials) guidelines. The total study duration is 12 months, with follow-up assessments scheduled at 3, 6, 9, and 12 months after baseline.

Sample Size Calculation:

Sample size was determined using G*Power software (version 3.1.9.4). A two-tailed independent-samples t-test was assumed with α = 0.05 and power = 0.95. The allocation ratio N1/N2 was set to 1. To detect a clinically meaningful difference in myopia progression between groups, a total of 210 participants are required, with 105 participants allocated to each treatment arm.

Randomization and Masking:

Eligible participants will be randomized in a 1:1 ratio to either the monotherapy group (atropine 0.05% alone) or the combination therapy group (atropine 0.05% plus bifocal spectacles). The randomization sequence will be generated using a computer-generated random number table. Allocation concealment will be maintained using sequentially numbered, opaque, sealed envelopes. Due to the nature of the interventions (eye drops vs. eye drops plus spectacles), masking of participants and care providers is not feasible. However, outcome assessors will be masked to group allocation.

Interventions:

Group A (Monotherapy): Participants receive atropine sulfate 0.05% ophthalmic solution. One drop is instilled in each eye once daily at bedtime. Parents or guardians are instructed on proper instillation technique, and compliance is monitored by counting returned empty bottles at each follow-up visit.

Group B (Combination Therapy): Participants receive atropine sulfate 0.05% ophthalmic solution (same dosage and regimen as Group A) PLUS bifocal spectacle correction. Bifocal spectacles are prescribed with the distance correction determined by cycloplegic refraction and a near addition of +2.00 D. Participants are instructed to wear spectacles during all waking hours.

Outcome Measures:

Primary Outcome: Change in spherical equivalent refraction (SER) from baseline to 12 months, measured using cycloplegic autorefraction. Cycloplegia is achieved with 1% cyclopentolate or 1% tropicamide administered 30 minutes prior to measurement.

Secondary Outcome: Change in axial length (AL) from baseline to 12 months, measured using optical biometry (e.g., IOLMaster or Lenstar). Three consecutive measurements are taken for each eye, and the mean value is used for analysis.

Safety Monitoring:

At each follow-up visit, participants are assessed for adverse events including:

Ocular: photophobia, blurred near vision, ocular irritation, conjunctival hyperemia, allergic reaction

Systemic: dry mouth, flushing, tachycardia, behavioral changes Adverse events are graded for severity and relationship to study intervention. Participants experiencing serious adverse events may be withdrawn from the study and referred for appropriate management.

Statistical Analysis:

All analyses will be performed using SPSS version 27 (IBM Corp., Armonk, NY, USA). Baseline characteristics will be summarized using descriptive statistics: mean and standard deviation for continuous variables, frequency and percentage for categorical variables. Normality of continuous data will be assessed using the Kolmogorov-Smirnov test. For between-group comparisons, independent t-tests will be used for normally distributed data; Mann-Whitney U tests will be used for non-normally distributed data. Within-group changes over time will be analyzed using repeated-measures ANOVA with Bonferroni correction for multiple comparisons. The primary analysis will be conducted on an intention-to-treat basis. A p-value < 0.05 will be considered statistically significant.

Ethical Considerations:

This study is conducted in accordance with the Declaration of Helsinki. Ethical approval has been obtained from the Institutional Review Board of The University of Faisalabad. Written informed consent is obtained from parents or legal guardians of all participants. Child assent is obtained when appropriate (age 7 years and above, depending on institutional policy). Participants and their families are informed of their right to withdraw from the study at any time without penalty or impact on their clinical care. Participant confidentiality is maintained throughout the study, and data are stored in a secure, password-protected database accessible only to authorized study personnel.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

210

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Punjab Province
      • Faisalābad, Punjab Province, Pakistan, 3800
        • The University of Faisalabad

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Children aged 4 to 16 years
  • Bilateral myopia with cycloplegic spherical equivalent refraction between -1.00 D and -6.00 D in each eye
  • Documented recent myopia progression of ≥ -0.50 D over the preceding 12 months
  • Best-corrected visual acuity (BCVA) of at least 6/12 (Snellen) or equivalent in each eye
  • Parent or guardian able and willing to provide written informed consent
  • Child assent when applicable (age 7 years and above per institutional policy)

Exclusion Criteria:

  • Ocular conditions affecting myopia progression: strabismus, amblyopia, significant astigmatism (>2.50 D), anisometropia (>2.50 D), cataract, glaucoma, uveitis, or history of ocular surgery
  • Prior myopia-control treatment within 6 months (atropine, orthokeratology, multifocal contact lenses, pirenzepine)
  • Known allergy or hypersensitivity to atropine or spectacle materials
  • Systemic or neurodevelopmental disorders affecting cooperation or refractive development
  • Inability to obtain accurate axial length or cycloplegic refraction measurements
  • Parent or guardian refusal to provide informed consent

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Atropine 0.05% Monotherapy
Participants receive atropine sulfate 0.05% ophthalmic solution, one drop in each eye once daily at bedtime, for 12 months.
Atropine sulfate 0.05% ophthalmic solution. One drop instilled in each eye once daily at bedtime. Parents or guardians are trained in proper instillation technique. Compliance is monitored by counting returned empty bottles at each follow-up visit (3, 6, 9, and 12 months).
Sperimentale: Combination Therapy (Atropine 0.05% + Bifocal Spectacles)
Participants receive atropine sulfate 0.05% ophthalmic solution (same regimen as Arm A) PLUS bifocal spectacle correction with distance correction based on cycloplegic refraction and +2.00 D near addition. Spectacles are to be worn during all waking hours.
Bifocal spectacle correction prescribed based on cycloplegic refraction for distance correction with a near addition of +2.00 Diopters. Spectacles are to be worn during all waking hours. Compliance is assessed through parental interview and observation at each follow-up visit.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mean Change in Spherical Equivalent Refraction (SER)
Lasso di tempo: Baseline and 12 months
Spherical equivalent refraction (SER) is calculated as sphere + (cylinder/2). Measurements are taken under cycloplegia achieved with 1% cyclopentolate or 1% tropicamide administered 30 minutes prior to measurement. An autorefractor is used to obtain three consecutive readings per eye; the mean value is used for analysis. SER is measured in diopters (D). A negative change indicates myopia progression (increase in myopia).
Baseline and 12 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mean Change in Axial Length
Lasso di tempo: Baseline and 12 months
Axial length is measured from the corneal apex to the retinal pigment epithelium using optical biometry (e.g., IOLMaster 500/700 or Lenstar LS 900). Three consecutive measurements are taken for each eye; the mean value is used for analysis. Axial length is measured in millimeters (mm). An increase in axial length indicates myopia progression.
Baseline and 12 months
Number of Participants with Treatment-Emergent Adverse Events
Lasso di tempo: Up to 12 months
Adverse events are assessed at each follow-up visit (3, 6, 9, and 12 months) through participant/parent interview and clinical examination. Adverse events are graded as mild, moderate, or severe and categorized as ocular (photophobia, blurred near vision, ocular irritation, conjunctival hyperemia, allergic reaction) or systemic (dry mouth, flushing, tachycardia, behavioral changes).
Up to 12 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

17 febbraio 2025

Completamento primario (Effettivo)

30 aprile 2026

Completamento dello studio (Effettivo)

15 maggio 2026

Date di iscrizione allo studio

Primo inviato

20 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

20 maggio 2026

Primo Inserito (Effettivo)

29 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

29 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

20 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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