Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Cognitive Dysfunction
  • Cognitive Impairment
  • Depression
  • Diabetic Retinopathy
Type
Observational
Design
Observational Model: Case-ControlTime Perspective: Cross-Sectional

Participation Requirements

Age
Between 65 years and 125 years
Gender
Both males and females

Description

A cross sectional study will be performed to determine correlation between retinal endpoints in persons with type 2 diabetes and cognitive impairment. 200 patients with type 2 diabetes without diabetic retinopathy and non to severe diabetic retinopathy. Primary objective: To determine whether struct...

A cross sectional study will be performed to determine correlation between retinal endpoints in persons with type 2 diabetes and cognitive impairment. 200 patients with type 2 diabetes without diabetic retinopathy and non to severe diabetic retinopathy. Primary objective: To determine whether structural and/or metabolic retinal markers are able to differentiate people with minimal cognitive impairment (MCI) within persons with type 2 diabetes (T2D). Secondary objective To assess whether retinal metabolism measured by oximetry can identify individuals with MCI among people with T2D. To assess whether retinal metabolism measured by oximetry can identify individuals with depressive symptoms among people with T2D. To determine whether retinal structural markers can identify people with depressive symptoms among people with T2D.

Tracking Information

NCT #
NCT04610749
Collaborators
Not Provided
Investigators
Principal Investigator: Frederik N Pedersen, M.D Department of Ophthalmology, OUH