Measuring Choroidal Thickness Using Optical Coherence Tomography

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age30-95
SponsorAssiut University

About this trial

To compare the choroidal thickness in eyes of diabetic patients with eyes of age matched controls using optical coherence tomography.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

All known Type 2 DM patients aged 30 to 95 years either gender who presented to ophthalmology clinics in Assuit ophthalmology hospital with no history of ocular treatment (ocular treatment naïve) and visual acuity of 0.1 (6/60) or more that are able to complete an eye examination, and non-diabetic healthy individuals (HbA1c <7) will be included in the study.

Disqualifiers

Known diagnosis of any other retinal disease, glaucoma, neurodegenerative disease, and any significant media opacities that precluded fundus imaging and not giving consent will be excluded.

Trial population

known Type 2 DM patients aged 30 to 95 years either gender with no history of ocular treatment and non-diabetic healthy individuals who come to the hosoital

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • optical coherence tomography

    Device

    measuring choroidal thickness using optical coherence tomography

Treatment groups

122 Participants
are divided into 2 treatment groups
Group A: diabetics1 intervention
Group B: non diabetics1 intervention

Trial outcomes

Primary outcomes

1

comparison between choroidal thickness

To compare choroidal thickness using optical coherence tomography between eyes of healthy individuals and diabetic patients without retinopathy

Time frame
2 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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