Long-term Ophthalmic Outcomes in Ex-premature Infants

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16+
SponsorErasmus Medical Center

About this trial

There is limited knowledge on ophthalmological outcomes in the adult population that was born prematurely. This study aims to evaluate the ophthalmic outcomes of ex-premature infants that have reached adolescence or adulthood.

Eligibility criteria

Qualifiers

Subjects eligible for ROP screening, and admitted to Erasmus MC between 1991 and 2007.

Disqualifiers

Subjects born after 2008,

Subject has passed away before the start of the study

Subject resides outside of the Netherlands

Subject has a physical or mental disability that makes it impossible to participate in a routine eye exam, or has a disability that classifies the subject as an incapacitated adult.

Trial design

Treatments tested in this trial

  • eye drops (Tropicamid)

Treatment groups

210 Participants
are divided into 1 treatment group

Sponsors and collaborators