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临床试验/NCT02710916
NCT02710916已完成不适用

SD-OCT Multimodal Analysis in GLaucoma

University Hospital, Bordeaux2 个研究点 分布在 1 个国家目标入组 109 人开始时间: 2016年2月22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
发起方
入组人数
109
试验地点
2
主要终点
Evaluation of Bruch's Membrane Opening Minimum Rim Width

研究概览

简要总结

Glaucoma is the first cause of irreversible blindness worldwide with more than 60 millions people affected in 2010. It is defined as a neurodegenerative disease characterized by a progressive loss of retinal ganglion cells (RGC), visual field deterioration and optic nerve excavation. Intraocular pressure (IOP) is the most common risk factor. Despite its severity, its impact on quality of life and an existing treatment that can delay visual field damages, there is no recommended strategy to screen the disease. Clinical evaluation of optic nerve head excavation performed either by ophthalmologists or glaucoma specialists is highly inter-observer dependent and limits its accuracy to diagnose glaucoma. Additionally, up to 30 to 40% of nerve fiber layer may be lost before detecting first visual field defects, thus making this tool not accurate enough for screening purposes.

Spectral-Domain Optical coherence tomography (SD-OCT) imaging technology allows precise and reproducible measurements of optic nerve head structures and retinal layers mainly related to the speed of acquisition and an axial resolution of 5 microns. New SD-OCT parameters have been developed to improve its diagnostic accuracy for glaucoma disease. The investigators therefore investigate performances of SD-OCT to discriminate glaucoma patients and controls. All subjects will undergo SD-OCT imaging (Spectralis™ OCT, Version 6.3, Heidelberg Engineering, Germany) and other study procedures in one single visit. All examinations performed on the subjects are non-significant risk.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Investigator)

入排标准

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

入选标准

  • Normal Subjects
  • No history or evidence of retinal pathology or glaucoma
  • Normal Humphrey 24-2 Visual Field (VF) : A mean defect (MD), corrected pattern standard deviation (CPSD) within 95% limits of normal reference, and glaucoma hemifield test (GHT) within normal limits (97%).
  • Intraocular pressure < 21 mm Hg
  • Open angle (Shaffer's grading system)
  • Normal appearing Optic Nerve Hypoplasia (ONH) and Nerve Fiber Layer (NFL) : intact neuroretinal rim without peripapillary hemorrhages, notches, localized pallor, or NFL defect
  • Symmetric ONH between left and right eyes: Cup-to-Disc Ratio (CDR) difference < 0.2 in both vertical and horizontal dimensions
  • Inclusion Criteria: Perimetric Glaucoma
  • ONH or NFL defect visible on slit-lamp biomicroscopy defined as one of following:
  • diffuse or localized thinning of the rim
  • disc (splinter) hemorrhage
  • notch in the rim
  • vertical cup/disc ratio greater than the fellow eye by > 0.2
  • Consistent glaucomatous pattern on both qualifying Humphrey Swedish Interactive Threshold Algorithm (SITA) 24-2 VF meeting at least one of the following quantitative criteria for abnormality:
  • PSD outside normal limits (p < 0.05)
  • GHT outside normal limits (p < 0.01)
  • Inclusion Criteria: Pre-Perimetric Glaucoma (PPG)
  • PPG participants must have at least one eye meeting all of the following criteria:
  • ONH or NFL defect visible on slit-lamp biomicroscopy defined as one of following:
  • diffuse or localized thinning of the rim
  • disc (splinter) hemorrhage
  • notch in the rim
  • well-defined peripapillary NFL bundle defect.
  • inter-eye vertical CDR asymmetry > 0.2
  • Baseline VF not meeting the criteria for the PG group.
  • Risk factors for glaucoma, one of following:
  • Intraocular pressure > 21 mm Hg
  • Family history of glaucoma

排除标准

  • Refractive error of > +6.00 D or < -6.00 D (SE), +3,00 D for astigmatism
  • Diabetic retinopathy
  • Other diseases that may cause VF loss or optic disc abnormalities
  • Inability to clinically view or photograph the optic discs due to media opacity or poorly dilating pupil
  • Inability to perform reliably on automated VF testing
  • Insufficient quality of Spectralis OCT images (this is not determined until after Spectralis OCT examination, and is an unusual circumstance). Minimum requirements are:
  • Retina completely included in image frame,
  • Quality Score ≥ 15 in the stored mean images,
  • Refusal of informed consent

研究组 & 干预措施

perimetric glaucoma patients

Sham Comparator

干预措施: SD-OCT Spectralis (Device)

perimetric glaucoma control patients

Sham Comparator

干预措施: SD-OCT Spectralis (Device)

preperimetric glaucoma patients

Active Comparator

干预措施: SD-OCT Spectralis (Device)

结局指标

主要结局

Evaluation of Bruch's Membrane Opening Minimum Rim Width

时间窗: 1 day

Diagnostic accuracy of SD-OCT to discriminate perimetric, preperimetric glaucoma patients and control patients

次要结局

  • Evaluation of Retinal Nerve Fiber Layer Thickness(1 day)

研究者

发起方
University Hospital, Bordeaux
申办方类型
Other
责任方
Sponsor

研究点 (2)

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