H52.1
Conditions
Interventions
Group 1: One-time collection of oral mucosa swabs
Sponsors
Universitätsklinik Freiburg, Klinik für Augenheilkunde
Eligibility
Sex/Gender
All
Age
8 Years to 15 Years
Inclusion criteria
Inclusion criteria: Participation in the AIM study, written informed consent obtained from the patient and his/her parents/legal guardians
Exclusion criteria
Exclusion criteria: No written informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlating a myopia risk score with the efficacy of low-dose atropine therapy | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlating other myopia and atropine related polymorphisms with the efficacy of low-dose atropine therapy | — |
Countries
Germany
Contacts
Public ContactNavid Farassat
Universitätsklinik Freiburg, Klinik für Augenheilkunde
Outcome results
None listed