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Search / Trial NCT02941263

Natural History of Geographic Atrophy Associated With Age-Related Macular Degeneration

Launched by NATIONAL EYE INSTITUTE (NEI) · Oct 20, 2016

Trial Information

Current as of June 06, 2025

Completed

Keywords

Eye Disease Natural History

ClinConnect Summary

Objective: Age-related macular degeneration (AMD), the leading cause of blindness in people over age 65 in the United States, is a heterogeneous clinical entity in which retinal degeneration occurs predominantly in the macula in the context of aging and leads to impairment of central visual acuity (VA). AMD occurs in two general forms, one of which involves choroidal neovascularization (CNV) with subsequent formation of a disciform scar. This is often referred to as the neovascular or wet form. A second form, the subject of this study, is termed dry atrophic macular degeneration or otherwis...

Gender

ALL

Eligibility criteria

  • * INCLUSION CRITERIA:
  • To be eligible, the following inclusion criteria must be met, where applicable.
  • 1. Participant must be 55 years of age or older.
  • 2. Participant must understand and sign the protocol s informed consent document.
  • 3. Participant must have evidence of early or intermediate AMD as defined by characteristic presence of drusen and/or pigmentary changes.
  • 4. Participant is enrolled in one of the following screening protocols: 08-EI-0102, 08-EI-0169 (closed), 08-EI-0043, 12-EI-0042, 11-EI-0147, or 16-EI-0134.
  • EXCLUSION CRITERIA:
  • A participant is not eligible if any of the following exclusion criteria are present.
  • 1. Participant is actively receiving study therapy in another investigational study.
  • 2. Participant is unable to comply with study procedures or follow-up visits.
  • 3. Participant is on ocular or systemic medications known to be toxic to the lens, retina or optic nerve (e.g., ethambutol, chloroquine, or hydroxychloroquine).
  • STUDY EYE ELIGIBILITY CRITERIA:
  • The participant must have at least one eye meeting all inclusion criteria and none of the exclusion criteria listed below.
  • STUDY EYE INCLUSION CRITERIA:
  • 1. The study eye(s) must have GA compatible with dry AMD. GA is defined as one or more well-defined and often circular patches of partial or complete depigmentation of the RPE, typically with exposure of underlying choroidal blood vessels. Even if much of the RPE appears to be preserved and large choroidal vessels are not visible, a round patch of RPE partial depigmentation may be classified as early GA. The GA in the study eye must be able to be photographed in their entirety and it must not be contiguous with any areas of peripapillary atrophy, which can complicate area measurements.
  • 2. The study eye(s) must have clarity of ocular media and degree of pupil dilation sufficient to permit adequate fundus photographs.
  • STUDY EYE EXCLUSION CRITERIA:
  • 1. Current evidence of neovascularization as determined by the treating physician or a history of treatments for neovascularization.
  • 2. Evidence of retinal atrophy due to causes other than atrophic AMD.
  • 3. Current evidence or history of ocular disorders in the study eye that might confound study outcome measures, including (but not limited to):
  • 1. non-proliferative diabetic retinopathy involving 10 or more hemorrhages or microaneurysms, or active proliferative diabetic retinopathy
  • 2. Branch or central retinal vein or artery occlusion
  • 3. Macular hole
  • 4. Pathologic myopia
  • 5. Uveitis
  • 6. Pseudovitelliform maculopathy
  • 4. History of vitreoretinal surgery.
  • 5. Need for ocular surgery during the course of the study.
  • 6. Recent history of lens removal (\< 3 months prior to enrollment) or Yttrium Aluminum Garnet (YAG) laser capsulotomy (\< 1 month prior to enrollment).

About National Eye Institute (Nei)

The National Eye Institute (NEI), part of the U.S. National Institutes of Health (NIH), is dedicated to conducting and supporting innovative research to understand, prevent, and treat eye diseases and vision disorders. As a leading sponsor of clinical trials, NEI aims to advance knowledge in ocular health through rigorous scientific inquiry and collaboration with researchers, healthcare professionals, and institutions. By fostering the development of new therapies and technologies, NEI plays a pivotal role in enhancing the quality of life for individuals affected by visual impairments and eye conditions.

Locations

Bethesda, Maryland, United States

Patients applied

0 patients applied

Trial Officials

Tiarnan DL Keenan, M.D.

Principal Investigator

National Eye Institute (NEI)

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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