Low-dose Atropine for Myopia Control in Children

Myopia, Progressive Clinical Trial

— AIM  

Official title:

Low-dose Atropine for Myopia Control in Children, a Prospective, Double-blind, Placebo-controlled, Multicentric, Randomized Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03865160
• Other study ID #: P001307
• Secondary ID: DRKS000233372020
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: October 19, 2021
• Est. completion date: April 2026

Study information

• Verified date: October 2022
• Source: University Eye Hospital, Freiburg
• Contact: Wolf Lagrèze, Prof.
• Phone: +49 (0) 761 270
• Email: wolf.lagreze[@]uniklinik-freiburg.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Myopia (nearsightedness) is the most common eye disorder. Only second to age, it is the main risk factor for major degenerative eye diseases such as glaucoma, macular degeneration or retinal detachment. Their risk increases with the degree of myopia. Hence, prevention of myopia and slowing its progression is of high relevance. Almost all clinical studies, including two large randomised clinical trials (RCT) were performed in Asia with Asian study participants. The results indicate that atropine eye drops can attenuate myopic progression in children, even in low concentrations thus minimizing unwanted side effects. However, the cumulative evidence is yet not strong enough to recommend their unrestricted use, especially in a Non-Asian population. We therefore intend to set up an adequately powered RCT comparing atropine 0.02% eye drops with placebo to validate previous findings and to test whether this therapeutic concept holds its promise in a European population.

Description:

Myopia (nearsightedness) is the most common developmental eye disorder in the first decades of life. It is the biggest risk factor for sight threatening degenerative eye diseases later in life, second only to age. Its prevalence is increasing worldwide in pandemic dimensions affecting now > 80% in Asian and > 40% in Caucasian populations. Myopia is one of the five eye diseases identified as immediate priorities by the WHO's global initiative for the elimination of avoidable blindness. It usually develops during primary school and its onset and progression are related to environmental factors such as near work and lack of day light exposure, to a lesser degree to genetic factors. Therefore, retardation of myopia progression is a major therapeutic goal. Clinical trials from Asia have shown that 0.01% atropine eye drops can attenuate progression of myopia while inducing only little side effects such as light sensitivity and reduced accommodation. Subsequent data also from Asia have suggested that a concentration of 0.05% atropine is slightly more effective with a still acceptable level of adverse effects. However, it is unclear whether this therapy is equally and sufficiently efficacious in a Caucasian population. It is also unclear which concentration of atropine represents the best compromise between efficacy and safety. Our own uncontrolled pilot data suggest that 0.01% delays progression by about 50% with negligible side effects, but that 0.05% induces a pupil dilation of > 3 mm, which is considered unacceptable. Due to the increasing prevalence also in Europe and an increasing demand from parents for means to retard myopia progression, the trial is the first European large scale randomized clinical trial investigating the safety and efficacy of 0.01% and 0.02% atropine eye drops in comparison to placebo drops. Such a trial is mandatory to substantiate the increasing off-label prescriptions of low-dose atropine in children and to develop clinical guidelines.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: April 2026
• Est. primary completion date: October 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 8 Years to 12 Years

Eligibility

Inclusion Criteria:

1. Male or female patients aged 8 to 12 years (up to the day before the 13th birthday)

2. Myopia of -1 D to -6 D with reported or documented annual progression = 0.5 D of myopia

3. Written informed consent obtained from patient (if applicable) and parents or legal guardians according to international guidelines and local laws

4. Ability to understand the nature of the trial and the trial related procedures and to comply with them

Exclusion Criteria:

1. Asian or African origin

2. Abnormal binocularity

3. Strabismus

4. Astigmatism >1.5 D

5. Anisometropia >1.5 D

6. History of amblyopia

7. Corrected visual acuity in any eye <0.63

8. Any acquired or developmental organic eye disease

9. Premature birth

10. Any known systemic metabolic disease or chromosomal anomaly

11. Previous use of any kind of contact lenses

12. Previous use of atropine eye drops

13. Epilepsy

14. Known hypersensitivity to the active substances or any of the excipients

15. Participation in any other interventional clinical trial within the last 30 days before the start of this trial

16. Simultaneous participation in other interventional trials which could interfere with this trial; simultaneous participation in registries and diagnostic trials is allowed

17. Contraindications according to the Summary of Product Characteristics (SmPC):

Increased intraocular pressure (primary forms of glaucoma or narrow angle glaucoma), chronic rhinitis sicca

18. Caution and pediatric counselling shall be assured if any of the following conditions are present according to the Summary of Product Characteristics (SmPC): Cardiac insufficiency, arrhythmia, coronary stenosis, hyperthyroidism, stomach or bowel stenosis, bowel paralysis, megacolon, muscle weakness, lung edema, hypersensitivity to atropine, spastic paralysis

19. Parents or children with poor understanding of the German language

20. Person who is in a relationship of dependence/employment with the sponsor or the investigator

Related Conditions & MeSH terms

• Myopia
• Myopia, Degenerative
• Myopia, Progressive

Intervention

Drug:
• Atropine eye drops, 0.01%
One drop of the above mentioned drug will be installed into each eye daily at bedtime.
• Atropine eye drops, 0.02%
One drop of the above mentioned drug will be installed into each eye daily at bedtime.
• Placebo (NaCl 0.9%) eye drops
One drop of the above mentioned drug will be installed into each eye daily at bedtime.

Locations

Country	Name	City	State
Germany	Augen-Zentrum-Nordwest, Augenpraxis Ahaus	Ahaus
Germany	Universitäts-Augenklinik Bonn	Bonn
Germany	Universitätsklinikum Erlangen, Augenklinik	Erlangen
Germany	Universitätsklinikum Essen, Klinik für Augenheilkunde	Essen
Germany	Medical Center - University of Freiburg, Eye Hospital	Freiburg
Germany	Universitätsmedizin Göttingen, Augenklinik	Göttingen
Germany	Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Augenheilkunde	Hamburg
Germany	Medizinische Hochschule Hannover, Klinik für Augenheilkunde	Hannover
Germany	Universitätsklinikum Heidelberg, Augenklinik	Heidelberg
Germany	Uniklinik Köln, Zentrum für Augenheilkunde	Köln
Germany	Universitätsklinikum Leipzig, Klinik und Poliklinik für Augenheilkunde	Leipzig
Germany	Universitätsklinikum Magdeburg A.ö.R., Universitätsaugenklinik	Magdeburg
Germany	Universitätsmedizin der Johannes Gutenberg-Universität Mainz, Augenklinik und Poliklinik	Mainz
Germany	Ludwig-Maximilians-Universität München, Augenklinik und Poliklinik	München
Germany	Klinik für Augenheilkunde des UKM, Gebäude D15	Münster
Germany	Pius-Hospital Oldenburg, Medizinischer Campus Universität Oldenburg, Universitätsklinik für Augenheilkunde	Oldenburg
Germany	AugenCentrum Rosenheim	Rosenheim
Germany	Universitätsklinikum Ulm, Klinik für Augenheilkunde	Ulm

Sponsors (1)

Lead Sponsor	Collaborator
University Eye Hospital, Freiburg

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Assessment of rebound of myopia progression (refraction) after cessation of atropine 0.02% treatment	Change in refraction [D/year] in year 3, to be determined only in the intervention group.	24-months - 36-months
Other	Assessment of rebound of myopia progression (axial length) after cessation of atropine 0.02% treatment	Change in axial length [mm/year] in year 3, to be determined only in the intervention group.	24-months - 36-months
Other	Change in refraction [D/year]	Change in refraction [D/year] after two years of treatment with low-dose atropine 0.02% eye drops (after year 2 in the interventional group) compared to low-dose atropine 0.01% eye drops (after year 3 in the control group).	intervention group: baseline - 24-months, control group: 12-months - 36-months
Other	Change in axial length [mm/year]	Change in axial length [mm/year] after two years of treatment with low-dose atropine 0.02% eye drops (after year 2 in the interventional group) compared to low-dose atropine 0.01% eye drops (after year 3 in the control group).	intervention group: baseline - 24-months, control group: 12-months - 36-months
Other	Assessment of safety of topical preservative free atropine in comparison to placebo with regard to pupil size	Pupil diameter in mm using the IOL Master 500 or 700 or a PlusoptiX device (preferred) at 200 - 300 lux room illumination. Parameter will be listed by site and patient and displayed in summary tables.	Baseline - 36-months
Other	Assessment of safety of topical preservative free atropine in comparison to placebo with regard to near vision	Visual acuity at near (40 cm distance) using Landolt-C near vision charts (non-crowded version) as decimal acuity. Parameter will be listed by site and patient and displayed in summary tables.	Baseline - 36-months
Other	Assessment of safety of topical preservative free atropine in comparison to placebo with regard to accomodation	Accommodation in D as the near point by the Royal air force near point rule (RAF) or by the Accommodation Convergence Rule (VISUS GmbH) (mean of three measurements of both eyes). Parameter will be listed by site and patient and displayed in summary tables.	Baseline - 36-months
Other	Assessment of safety of topical preservative free atropine in comparison to placebo with regard to pulse rate	Pulse rate (per minute): parameter will be listed by site and patient and displayed in summary tables.	Baseline - 36-months
Other	Number of participants with treatment-related adverse events as assessed by the current CTCAE v4.0	A questionnaire about potential side effects will be completed three times during the study course; A patient diary of potential side effects will be provided for patients/parents or guardians to complete and bring to each study visit; Adverse events will be documented in the eCRF; The adverse events are displayed in summary tables by treatment.	Baseline - 36-months
Primary	Demonstration of superiority of low-dose atropine 0.02% eye drops compared to placebo for myopia control	Change in cycloplegic refraction [dioptre (D)/year] after one year will be performed using an analysis of covariance (ANCOVA) model with the annual change in refraction as the dependent variable. The mean value of both eyes is analysed.	Baseline - 12 months
Secondary	Assessment of axial eye length growth under low-dose atropine 0.02% in comparison to placebo	Change in axial length [mm/year]. The mean value of both eyes is analysed. Analyses will be performed in a regression model.	Baseline - 12 months
Secondary	Assessment of the categorized rate of change in refraction of low-dose atropine 0.02% compared to placebo	The primary endpoint change in cycloplegic refraction after one year will be categorized (patients progressing < 0.25D (dioptre), 0.25D - 0.75D and > 0.75D after one year of treatment) and will be analysed descriptively, giving absolute and relative frequencies of these categories as a supportive analysis.	Baseline - 12 months

External Links

•   Homepage of AIM (German language)