Atropine Sulfate 0.05% Oph Soln
DrugAtropine Sulfate 0.05% Oph Soln compounded at the pharmacy
NCT Number: NCT07567040
The aims of this clinical trial will test whether or not the onset of nearsightedness is delayed in a group of children randomized to nightly drops in 0.05% atropine in both eyes, in comparison to children who receiving nightly placebo drops in both eyes. The primary outcome is the two-year cumulative incidence of nearsightedness. The second aim of this project will determine whether atropine is associated with slower eye growth in children receiving nightly drops of atropine versus placebo.
Interested in participating?
Request Info6 year–11 year
All sexes
Interventional
Phase 3
University of Alabama School of Optometry, Birmingham, Alabama, United States
The "Delaying the Onset of Nearsightedness (DONUT) Study - Data Coordinating Center" is a randomized clinical trial designed to compare the effectiveness 0.05% atropine and a placebo in delaying the onset of nearsightedness. It is a multicenter (14 clinic centers) randomized clinical trial of 606 children (recruited over two years) ages 6 to 11 years who are determine to be at high risk of myopia onset, as measured by cycloplegic autorefraction and age. The primary outcome is the two-year cumulative incidence of myopia. The second aim of this project will determine whether atropine is associated with slower axial elongation in children receiving nightly drops of atropine versus placebo.
Participants will be seen every six months for at least two years to determine the onset of myopia.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Atropine Sulfate 0.05% Oph Soln compounded at the pharmacy
Placebo drop with same formulation as treatment minus the atropine
Time frame: Two years
Cumulative incidence of myopia as measured by cycloplegic autorefraction comparison between treatment and placebo
Time frame: Two years
Axial elongation comparison between treatment and placebo
Time frame: 2 years
A comparison of the time to myopia onset between the treatment and placebo groups
Time frame: 2 years
Spherical equivalent progression (change) comparison between treatment and placebo
Contact information is provided by the study sponsor or research team.
Ohio State University
Other
Acronym: DONUT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07316998
Eye Diseases, Myopia
Paris, France
View Trial DetailsNCT07698977
Eye Diseases, Myopia
Budapest, Hungary
View Trial DetailsNCT07512102
Eye Diseases, Myopia
Guangzhou, Guangdong, China
View Trial DetailsNCT07512115
Eye Diseases, Myopia
Guangzhou, Guangdong, China
View Trial Details