Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

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

20. mai 2026 oppdatert av: 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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

210

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: 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).
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean Change in Spherical Equivalent Refraction (SER)
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean Change in Axial Length
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

17. februar 2025

Primær fullføring (Faktiske)

30. april 2026

Studiet fullført (Faktiske)

15. mai 2026

Datoer for studieregistrering

Først innsendt

20. mai 2026

Først innsendt som oppfylte QC-kriteriene

20. mai 2026

Først lagt ut (Faktiske)

29. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

20. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere