About this trial
To study the possible correlation between pupillary diameter before and after dilation with intraocular pressure, lens stability and glaucomatous damage (represented by optic disc changes using cup to disc ratio and OCT changes in retinal nerve fiber layer and ganglion cell complex) in each eye of the same patient with PEX.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All patients with pseudoexfoliation syndrome.
Disqualifiers
previous ocular surgery or ocular trauma affecting the pupil. Any systemic or neurologic disease affecting the pupil
Trial population
All patients with pseudoexfoliation syndrome
Trial design
Other
Cross-sectional
Treatments tested in this trial
optical coherence tomography
DeviceOptical coherence tomography (OCT) is a non-invasive imaging test . It uses light waves to take cross-section pictures of the retina . With OCT, the ophthalmologist can see each of the retina's distinctive layers, and so we can use it to study the changes in pseudoexfoliation syndrome.
Treatment groups
Trial outcomes
Primary outcomes
To study the possible correlation between pupillary diameter before and after dilation with intraocular pressure, lens stability and glaucomatous damage
in each eye of the same patient with PEX we study the correlation between the pupillary size before and after dilation with intraocular pressure, lens stability and glaucomatous damage represented by optic disc changes (cup to disc ratio) and OCT changes (RNFL and GCC).
Locations
Sponsors and contacts
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