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临床试验/NCT06381596
NCT06381596已完成不适用

Retinal Fundus Flavoprotein Fluorescence in Age Related Macular Degeneration: New Insights From Multimodal Imaging

University of Wisconsin, Madison1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2024年4月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
1
主要终点
Optical Coherence Tomography (OCT) Variables

研究概览

简要总结

The goal of this clinical trial is to learn if the areas of stressed cells in the retina correlate to areas of disease identified in standard imaging and whether the images are helpful to identify potential areas of concern before symptoms or disease occurs. The main question it aims to answer is:

  • to evaluate patterns of increased autofluorescence FPF in the setting of geographic atrophy

Participants will undergo FPF imaging using the OcuMet Beacon system.

详细描述

The goal of this clinical trial is to learn if areas of mitochondrial functional distress in the macula (as imaged using fundus flavoprotein fluorescence) correlate with areas of anatomic disease identified on standard fundus autofluorescence (FAF) imaging.

The study aims to evaluate patterns of anomalous fundus flavoprotein fluorescence (FPF) in patients with advanced geographic atrophy (GA) due to dry age-related macular degeneration.

Participants will undergo FPF imaging using the OcuMet Beacon system and FAF imaging using Heidelberg Spectralis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •50 years or older and may be either male or female of any race
  • •Established diagnosis of GA due to AMD
  • •GA characteristics: GA area of between 1.25 mm² and 23 mm², with seventy percent of eyes having GA area ranging from 2.5 mm2 to 17.5 mm
  • •GA may be unifocal or multifocal. GA may be subfoveal or extrafoveal, with twenty-five percent of eyes having subfoveal GA. The presence of concurrent peripapillary atrophy will not exclude subjects from participation
  • •Willing to participate as evidenced by signing the written informed consent

排除标准

  • •Unable to tolerate ophthalmic imaging
  • •Presence of neovascular AMD on OCT as confirmed by an ophthalmologist
  • •Presence of significant media opacity preventing adequate retinal imaging
  • •Presence of concurrent retinal disease which may confound assessment

研究组 & 干预措施

Fundus autofluorescence (FAF) imaging

Experimental

干预措施: OcuMet Beacon (Device)

结局指标

主要结局

Optical Coherence Tomography (OCT) Variables

时间窗: up to 45 minutes

Ellipsoid Zone (EZ) loss refers to damaged photoreceptors in the eye. Retinal Pigment Epithelium (RPE) are cells that nourish photoreceptors in the eye, RPE loss is a measure of the degradation of these cells. Geographic Atrophy (GA) is an advanced stage of macular degeneration. These OCT variables are measured in millimeters squared from images taken with the Heidelberg Spectralis.

Flavoprotein Fluorescence (FPF) Intensity

时间窗: Up to 45 minutes

Average pixel intensity over a 5.5 mm-diameter region centered at the macula, a measure of oxidative stress. Data range from 0-100 where higher numbers indicate more severe disease. This is measured with the OcuMet Beacon.

FPF Heterogeneity

时间窗: up to 45 minutes

This is a measure of variability in retinal mitochondrial flavoprotein fluorescence (FPF) across the macula. It is a parameter that measures distribution and spatial variability of fluorescent signal by quantifying signal distribution of energy in localized hotspots, normalized to background. Normal values are less than 1 AU (arbitrary units), with values higher than 1 AU (in the range of 1-10 AU) corresponding to increased levels of metabolic distress due to oxidized mitocondria within the particular area of the retina that was imaged. This is measured with the OcuMet Beacon.

Correlation Between FPF-intensity, FPF-heterogeneity and OCT Continuous Variables

时间窗: up to 45 minutes

Spearman's rank coefficient was chosen as the primary metric due to the relatively small number of eyes in our sample as well as the lack of normally-distributed data (confirmed by Shapiro-Wilk tests, evaluated at α=0.05). Correlations were calculated between both FPF biomarkers and all FAF/OCT variables (i.e. areas of GA, EZ loss, and RPE loss). To account for correlation between eyes belonging to the same patient, p-values were obtained via nonparametric bootstrap resampling at the patient level.

次要结局

  • Compare the Cross-sectional Associations Between FPF Intensity to FAF Area at the Time of Measurement(Up to 45 minutes)
  • Compare the Cross-sectional Associations Between Best Corrected Visual Acuity (BCVA - Using Early Treatment Diabetic Retinopathy Study, Greater Number of Letters Read Correctly Equals Better Vision) to FAF Area at the Time of Measurement(Up to 45 minutes)
  • Correlation Between FPF-intensity, FPF-heterogeneity and Participant Variables(up to 45 minutes)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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