Inhibition of myopic progression with using atropine eye drop. Myopia
Conditions
Interventions
Intervention 1: Intervention group 1: Receive 0.1% atropine eye drops. Intervention 2: Intervention group2: Receive 0.01% atropine eye drops. Intervention 3: Control group: receive artificial tear e
Sponsors
Guilan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
6 Years to 18 Years
Inclusion criteria
Inclusion criteria: aged 6-18 Myopia astigmatism (2-6 diopter) No amblyopia
Exclusion criteria
Exclusion criteria: Age under 6 and over 18 Amblyopia Strabismus
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percent of myopic power and axial length changes. Timepoint: 6 months after discontinuation of atropine 0.1% and 0.01% eye drop and placebo. Method of measurement: Auto refractometer and ultrasound. | — |
Secondary
| Measure | Time frame |
|---|---|
| Myopic power and axial length changes 6 months after treatment withdrawal. Timepoint: 6 months after discontinuation of atropine 0.1% and 0.01% eye drop and. Method of measurement: Auto refractometer and ultrasound. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAbdolreza medghalchi
Guilan University of Medical Aciences
Outcome results
None listed