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Atropine 0.01% Eyedrops for Evolutive Myopia Treatment in Children

Atropine 0.01% Eyedrops for Evolutive Myopia Treatment in Children. MYOPSTOP

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04252989
Enrollment
50
Registered
2020-02-05
Start date
2019-12-18
Completion date
2027-12-31
Last updated
2025-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Children, Myopia

Keywords

atropine

Brief summary

Prevalence of myopia and its complications has been increasing over the past decades, especially among children and adolescents. It reaches record levels in Asia: nearly 80% of the population in some regions in 2012 where the investigators speak in terms of epidemic. ATROPINE 0.01% eyedrops one drop per day is today an evolutive myopia treatment, whose results are promising. The investigators use this eye drops in our clinical practice at hospital of Saint-Etienne since 2017. Few clinical data have been published so far concerning the French population. The investigators would like to build a database so that the investigators can publish our results and share our experience.

Interventions

OTHERdata collection

* Demographic data: age, sex * Ophthalmological history: refraction of parents, previous refractions * Ophthalmological data at each examination: intra-ocular pression, objective refraction after fog, cycloplegia with SKIACOL, slit lamp, dilated eye exam, biometrics * Potential undesirable events (halos, photophobia...)

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* Children with active myopia treated with ATROPINE 0.01% eye drops * patient affiliated with a social security organization * agreement of both parents

Exclusion criteria

* non compliance with treatment

Design outcomes

Primary

MeasureTime frameDescription
biometricsevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
previous refractionsevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
refraction of parentsevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
intra-ocular pressionevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
objective refraction after fogevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
cycloplegia with SKIACOLevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
slit lampevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice
dilated eye examevery 6 months up to age 18 yearseffectiveness of ATROPINE 0.01% eyedrops in our current clinical practice

Secondary

MeasureTime frameDescription
undesirable events collectionevery 6 months up to age 18 yearsmeasured the tolerance of ATROPINE 0.01% eyedrops. Number of participants with treatment-related adverse events.

Countries

France

Contacts

Primary ContactMarie Caroline TRONE
m.caroline.trone@chu-st-etienne.fr04 77 82 94 28
Backup ContactMarie PEURIERE
marie.peuriere@chu-st-etienne.fr04 77 82 92 72

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026