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Search / Trial NCT03233646

Retinal Imaging in Neurodegenerative Disease

Launched by DUKE UNIVERSITY · Jul 26, 2017

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

Oct Angiography (Octa) Optical Coherence Tomography (Oct) Vessel Density Superficial Capillary Plexus Retinal Microvasculature Scanning Laser Ophthalmoscopy Ultra Widefield (Uwf) Imaging Perfusion Density Retinal Nerve Fiber Layer Ganglion Cell Inner Plexiform Layer Choroidal Vascularity Index

ClinConnect Summary

This clinical trial, titled "Retinal Imaging in Neurodegenerative Disease," is focused on using advanced imaging techniques to better understand eye health in people with various brain disorders, including Alzheimer's Disease, Parkinson's Disease, and Mild Cognitive Impairment, among others. The goal is to find new ways to measure changes in the eye that may help doctors understand how these diseases affect patients. Researchers will use non-invasive methods like optical coherence tomography (OCT) and ultra-widefield fundus photography, which are safe and painless ways to take detailed pictures of the retina, the light-sensitive layer at the back of the eye.

Adults aged 65 to 74 with or without neurodegenerative diseases may be eligible to participate in this study. Participants will undergo imaging tests that don't require any surgery, making it a low-risk option for individuals. It’s important to note that anyone who has had significant eye surgery, other than cataract surgery, may not be able to join. If you're selected, you can expect to help researchers gather valuable information that could lead to better understanding and treatment of these conditions in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Adults with neurodegenerative disease ((MCI, PD, AD, FTD, DLB, ALS, MS, HD, TBI, concussion, PTSD and other neurodegenerations as well as Down Syndrome)
  • Adults without neurodegenerative disease
  • Exclusion Criteria:
  • Inability to cooperate with or complete testing or other neurologic or age- related ocular conditions that would impact image acquisition.
  • Eyes that have had intraocular surgery, other than cataract surgery.
  • If two eyes satisfy the inclusion criteria, both eyes will be included in the study. If one eye satisfies the inclusion criteria, the eye that qualifies will be included in the study.

About Duke University

Duke University, a leading academic and research institution located in Durham, North Carolina, is renowned for its commitment to advancing healthcare through innovative clinical research. With a strong emphasis on interdisciplinary collaboration, Duke conducts a wide array of clinical trials aimed at developing cutting-edge therapies and improving patient outcomes across various medical fields. The university's Clinical Research Institute provides comprehensive support for trial design, implementation, and regulatory compliance, ensuring that all research adheres to the highest ethical and scientific standards. Duke’s dedication to translating research findings into effective clinical practices underscores its role as a pivotal contributor to the global medical community.

Locations

Durham, North Carolina, United States

Durham, North Carolina, United States

Patients applied

0 patients applied

Trial Officials

Sharon Fekrat, MD FACS FASRS

Principal Investigator

Duke University

Dilraj Grewal, MD

Principal Investigator

Duke University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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