Myopia
RecruitingSafety and Efficacy of Sodium Phenylbutyrate Eye Drops in Children with Myopia
- Disease:Myopia
- Substances:Sodium Phenylbutyrate
Austria- Participants:0–17 years
- Substances:Sodium Phenylbutyrate
- Sponsor:Laboratoires Thea
Rare diseases
Investigational molecules
Locations
A plain-language summary of the goals, design and what participants do
This study aims to assess the effect of brimonidine eye drops 0.025% on the progression of myopia (nearsightedness) in children. Myopia is a common vision condition where close objects appear clear, but distant objects appear blurry. The purpose is to determine how brimonidine eye drops affect the progression of myopia over a two-year period and measure changes in the refractive status of the eye.
The research involves children aged 6 to 14 years who have myopia of at least -1.50 diopters (a unit of measurement for the focusing power of the eye). During the study, participants will receive brimonidine eye drops, and their eye measurements will be taken every six months to track any changes in their vision. These measurements include the axial length (the distance from the front to the back of the eye), visual acuity (sharpness of vision), and other eye characteristics.
The study will monitor various aspects of eye health including pupillometry (measurement of pupil size under different lighting conditions), accommodation (how well the eye adjusts focus), corneal topography (mapping the surface curvature of the cornea), and intraocular pressure (pressure inside the eye). Throughout the study, safety will be assessed by collecting information about any adverse events.
The trial runs in 5 steps – from screening to follow-up. Each step says what happens and what the team monitors.
9 criteria
12 criteria
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