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Atropine eyedrops for treatment of increasing shortsight

Low strength Atropine (0.01%) eyedrops for treatment of progressive myopia in children and young adults-A Randomised Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021538
Enrollment
50
Registered
2019-10-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: H521- Myopia

Interventions

Intervention1: Atropine: 0.01% Atropine eyedrops HS only in the randomised eye for 1 year Control Intervention1: NIL: Other eye is not treated and will be used as the comparator to the treated eye.The

Sponsors

Dr Abraham Kurian
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children or Young adults in the age group 5-15 years. 2. Myopic refractive error of spherical equivalent > 1.00D as measured by cycloplegic refraction 3. Astigmatism of 4. Documented progression of myopia 5. Ability to understand and follow the study instructions you receive and likely to be amenable for 1 year followup. 6. Normal ocular health other than refractive error 7. Normal Intraocular pressure (

Exclusion criteria

Exclusion criteria: 1. Known Allergy or hypersensitivity to Atropine, Cyclopentolate, Phenyl ephrine or Proparacaine 2. Amblyopia in atleast one eye 3. History of significant cardiac or respiratory illness 4. Current enrolment in another investigational study or participation in such a study within 30 days of entry into this study 5. No previous or current use of contact lenses or bifocals or progressive lenses or other forms of treatment (including Atropine in any strength) for myopia 6. Patient has a condition or situation which in the investigators opinion, may put the patient at a significant risk, may confound the study results, or interfere with the participation in the study.

Design outcomes

Primary

MeasureTime frame
Progression of myopia in terms of Spherical equivalent in realtion to baselineTimepoint: 1 year

Secondary

MeasureTime frame
Change in axial length with respect to the baseline measurement.Timepoint: 1 year

Countries

India

Contacts

Public ContactDr Abraham Kurian

Chaithanya Eye Hospital and Research Institute, Kesavadasapuram, Trivandrum

abrahamkurian55@yahoo.in9847094478

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026