Biomarker of Diabetic Retinopathy

Sponsor
Indiana University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05079399
Collaborator
(none)
192
3
53.9
64
1.2

Study Details

Study Description

Brief Summary

Diabetic retinopathy (DR) is a complication of diabetes in which blood vessels supplying blood to the back of the eye (retina) are dysfunctional. This can lead to an improper supply of oxygen and nutrients to the retinal tissue, or it may trigger the formation of new blood vessels in response to the oxygen/nutrient deficiency. Ultimately affecting the normal vision. There is no known marker that will provide information on the health status of retinal blood vessels. Using highly specialized cells in the blood, this study will try to discover a marker of DR.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood draw

Study Design

Study Type:
Observational
Anticipated Enrollment :
192 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Biomarker of Diabetic Retinopathy
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Jun 30, 2026
Anticipated Study Completion Date :
Jun 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Healthy Control

Other: Blood draw
Blood samples will be collected via venipuncture

Diabetes but no retinopathy

Other: Blood draw
Blood samples will be collected via venipuncture

Mild non proliferative diabetic retinopathy

Other: Blood draw
Blood samples will be collected via venipuncture

Moderate non proliferative diabetic retinopathy

Other: Blood draw
Blood samples will be collected via venipuncture

Severe non proliferative diabetic retinopathy

Other: Blood draw
Blood samples will be collected via venipuncture

Proliferative diabetic retinopathy

Other: Blood draw
Blood samples will be collected via venipuncture

Outcome Measures

Primary Outcome Measures

  1. mRNA and miRNA sequencing of circulating angiogenic cells isolated from study participants [Baseline and change in RNA signature in follow up visit (between 3-5 years)]

  2. Surface marker expression of inflammatory markers using flow cytometry [Baseline]

  3. miRNA expression [Baseline]

  4. Epigenetic changes in circulating angiogenic cells with different severities of diabetic retinopathy [Baseline]

Secondary Outcome Measures

  1. Early Treatment Diabetic Retinopathy Study (ETDRS) clinical scoring in wide-field fundus photography [Baseline and follow up visit (between 3-5 years)]

    The scoring will be between 10 (no retinopathy) and 85 (advanced proliferative diabetic retinopathy). Higher score means worst outcome

  2. Presence or absence of neovascularization and total area of non-perfusion in fluorescein angiography (FA) [Baseline and follow up visit (between 3-5 years)]

  3. Change in vessel density in optical coherence tomography angiography (OCT-A) [Baseline and follow up visit (between 3-5 years)]

  4. Change in retinal thickness in optical coherence tomography angiography (OCT-A) [Baseline and follow up visit (between 3-5 years)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Ability to cooperate with imaging procedures.

  • Health status: established type 2 diabetes

  • No history of panretinal photocoagulation (PRP)

  • No history of treatment with intravitreal agents for past 12 months

Exclusion Criteria:
  • Previous or current malignancy

  • Acute or chronic infection (HIV, hepatitis B or C, tuberculosis)

  • Cerebral vascular accident or cerebral vascular procedure

  • Current pregnancy

  • History of organ transplantation

  • Presence of a graft (to avoid any effect of the graft)

  • History of previous vitrectomy

  • Subjects with a history of age-related macular degeneration age-related macular degeneration (AMD), glaucoma, uveitis, and branched or central vein occlusion.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Spring Mill Clinic Carmel Indiana United States 46920
2 Eskenazi Eye Clinic Indianapolis Indiana United States 46202
3 Glick Eye Institute Indianapolis Indiana United States 46202

Sponsors and Collaborators

  • Indiana University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ashay Bhatwadekar, PhD, RPh, Associate Professor Ophthalmology, Indiana University
ClinicalTrials.gov Identifier:
NCT05079399
Other Study ID Numbers:
  • 11656
First Posted:
Oct 15, 2021
Last Update Posted:
Jan 20, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 20, 2022