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Atropine eyedrops for preventing increase in refractive error (shortsight and astigmatism)

Low strength atropine (0.01%) eyedrops for preventing progression of Compound Myopic Astigmatism in children and young adults- A Randomised Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/018970
Enrollment
50
Registered
2019-05-07
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: H522- Astigmatism

Interventions

Intervention1: Atropine: Atropine 0.01% eyedrops 1 drop HS in the randomised eye for 1 year Control Intervention1: NIL: Atropine eyedrops will be used only in one eye of each patient.Te other eye will

Sponsors

DrAbraham 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 > 1.50D as measured by cycloplegic refraction 4. Documented progression of myopic component of Compound Myopic astigmatism 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
The primary outcome will be progression of the myopic component of Compound Myopic astigmatism estimated as the change in spherical equivalent refractive error relative to the baselineTimepoint: 1 year

Secondary

MeasureTime frame
The secondary outcome will be the change in axial length with respect to the baseline measurement.Timepoint: 1 year

Countries

India

Contacts

Public ContactDr Iodine Reghunadhan

Chaithanya Eye Hospital and Research Institute

iodine_b@yahoo.com

Outcome results

None listed

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