Clinical Trials Directory

Trials / Completed

CompletedNCT04112667

Functionally Validated Structural Endpoints for Early AMD

Status
Completed
Phase
Study type
Observational
Enrollment
556 (actual)
Sponsor
Cynthia Owsley · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Accepted

Summary

Delayed rod-mediated dark adaptation (RMDA), or delayed recovery of vision in a dark environment, is a functional biomarker (i.e., risk factor) for early age-related macular degeneration (AMD). This research plan is designed to elucidate the structural (anatomical) basis of this visual deficit using cellular- and subcellular level imaging of the retina and its supporting tissues in living people. An accurate map and timeline of structure-function relationships in persons tested for night vision will result in functionally validated structural endpoints for early AMD trials, as well as define major biologic effects for development into future treatments.

Detailed description

The Alabama Study on Early Age-Related Macular Degeneration 2 (ALSTAR2) is a prospective cohort study with baseline measurements that are repeated at follow-up 3 years later. The baseline and 3 year follow-up visits will each consist of 2 visits for a total of 4 visits. Study assessments are listed below. All are collected at two visits at both baseline and follow-up for 4 visits total (blood collection for DNA analysis at baseline only). For some functional tests (photopic and mesonic acuity, photopic and mesonic contrast sensitivity), each eye will be tested separately. For other functional tests (dark-adapted two-color perimetry, light-adapted cone-mediate perimetry, rod-mediated dark adaptation), only one eye will be tested, which will be designated by the study eye. Tropicamide 1% and phenylephrine hydrochloride 2.5% are used to dilate pupils (diameter of ≥ 6 mm) as needed for specific parts of the protocol. After completing the baseline visits, participants will receive an annual phone call from the study coordinator so that contact information can be updated. Participants will receive an annual newsletter containing study related information (this will be submitted to the IRB for approval). Study Assessments: 1. Rod-mediated dark adaptation (RMDA), the ability to recover light sensitivity after exposure to a bright light. 2. Dark-adapted two-color microperimetry, a measure of light sensitivity for lights of two different colors. 3. Photopic and mesopic acuity in central vision, as measured by letter charts.. 4. Photopic and mesopic contrast sensitivity in central vision, as measured by letter charts.. 5. Multimodal ocular imaging on both eyes, which consists of the following: color fundus photography, spectral domain optical coherence tomography (SDOCT), blue fundus autofluorescence (standard and quantitative), OCT-angiography (OCT-A). 6. Blood draw for the analysis of C-reactive protein, high-density lipoprotein, carotenoid level, DNA extraction, and examination of the presence of genetic risk associated with age-related macular degeneration (AMD). 7. Questionnaires: Demographics, medical co-morbidities, cognitive status screen, medication use, alcohol use, smoking, self-reported visual difficulty in the visual activities of daily living The Young normal group will only complete: 1. Rod-mediated dark adaptation (RMDA), the ability to recover light sensitivity after exposure to a bright light. 2. Dark-adapted two-color microperimetry, a measure of light sensitivity for lights of two different colors. 3. . Photopic and mesopic acuity in central vision, as measured by letter charts.. 4. Photopic and mesopic contrast sensitivity in central vision, as measured by letter charts.. 5. Multimodal ocular imaging on both eyes, which consists of the following: color fundus photography, spectral domain optical coherence tomography (SDOCT), blue fundus autofluorescence (standard and quantitative),OCT-angiography (OCT-A).d and quantitative), OCT-angiography.

Conditions

Interventions

TypeNameDescription
OTHERNormal Macular HealthThis group of participants will have function assessed using rod- and cone-mediated tests (rod-mediated dark adaptation, 2 color dark adapted perimetry, cone-mediated perimetry, photopic and mesopic acuity, photopic and mesopic contrast sensitivity). Age-related macular degeneration status will be determined by multi-modal imaging.
OTHEREarly Macular DegenerationThis group of participants will have function assessed using rod- and cone-mediated tests (rod-mediated dark adaptation, 2 color dark adapted perimetry, cone-mediated perimetry, photopic and mesopic acuity, photopic and mesopic contrast sensitivity). Age-related macular degeneration status will be determined by multi-modal imaging.
OTHERYoung NormalsThis group of participants will have function assessed using rod- and cone-mediated tests (rod-mediated dark adaptation, 2 color dark adapted perimetry, cone-mediated perimetry, photopic and mesopic acuity, photopic and mesopic contrast sensitivity). Age-related macular degeneration status will be determined by multi-modal imaging.

Timeline

Start date
2019-10-07
Primary completion
2024-07-01
Completion
2024-10-31
First posted
2019-10-02
Last updated
2025-09-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04112667. Inclusion in this directory is not an endorsement.