Myopia Progression Control Using Atropine 0.05% After Pediatric Cataract Surgery And Intraocular Lens Implantation Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-7
SponsorCairo University

About this trial

Myopic shift remains a debilitating and unpredictable adverse event following pediatric cataract surgery. While research exploring peripheral myopic defocus for post-cataract surgery myopia prevention shows promising results, the use of multifocal intra-ocular lenses (IOLs) cannot be used liberally in countries with high disease burden and challenged economies due to high price and decreased availability. To date there are no studies evaluating the use of topical atropine for the management of myopic shift following pediatric cataract surgery.

The investigators aim to explore the use of 0.05% topical atropine in the prevention and management of myopic shift following pediatric cataract surgery.

Eligibility criteria

Qualifiers

Children after IOL implantation (primary or secondary)

Age 1-7 years

Disqualifiers

Eyes with post-operative media opacity hindering adequate assessment of refraction

Eyes with complicated surgeries (e.g. vitreous loss, dropped lens matter requiring PPV, retinal detachment, etc)

Retinal pathologies

Glaucoma (congenital or secondary to surgery)

Trial design

Treatments tested in this trial

  • Atropine Eye drops

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators