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Atropine eyedrops for treatment of increasing shortsight

Phase 4
Conditions
Health Condition 1: H521- Myopia
Registration Number
CTRI/2019/10/021538
Lead Sponsor
Dr Abraham Kurian
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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 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 ( <21 mm Hg)

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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Progression of myopia in terms of Spherical equivalent in realtion to baselineTimepoint: 1 year
Secondary Outcome Measures
NameTimeMethod
Change in axial length with respect to the baseline measurement.Timepoint: 1 year
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