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Evaluation of the Retina of Subjects Without Diabetes Mellitus and Subjects With Diabetes Mellitus Without Diabetic Retinopathy Using Optical Coherence Tomography

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Johns Hopkins University

Status

Completed

Conditions

Diabetic Retinopathy

Treatments

Other: OCT Imaging both Normal and diabetic groups

Study type

Observational

Funder types

Other

Identifiers

NCT01946997
03-11-05-03

Details and patient eligibility

About

The purpose of this study is to evaluate topographic features of the posterior pole of the eye in normal subjects as well as in subjects with diabetes mellitus but without diabetic retinopathy (DR) using optical coherence tomography (OCT). The investigators proposal is a novel study to determine retinal volume of normal and diabetic subjects without DR. Specifically, the investigators will establish a standardized reference range for retinal thickness and volume that will provide standards for OCT analysis of different clinical trials for retinal diseases.

Enrollment

200 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy retinas
  • Willingness to sign informed consent to have OCT images taken.

Exclusion criteria

  • No macular pathology
  • No Diabetes

Trial design

200 participants in 2 patient groups

Group 1: Non Diabetic
Description:
Normal retina
Treatment:
Other: OCT Imaging both Normal and diabetic groups
Group 2: Diabetes with no retinopathy
Description:
Diabetic patients without diabetic retinopathy
Treatment:
Other: OCT Imaging both Normal and diabetic groups

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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