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临床试验/NCT01440660
NCT01440660已完成不适用

Phenotypes of Nonproliferative Diabetic Retinopathy in Diabetes Type 2 Patients Identified by Optical Coherence Tomography, Colour Fundus Photography, Fluorescein Leakage and Multifocal Electrophysiology (DIAMARKER Project: Genetic Susceptibility for Multi-systemic Complications in Diabetes Type-2: New Biomarkers for Diagnostic and Therapeutic Monitoring).

Association for Innovation and Biomedical Research on Light and Image1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2012年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Multimodal testing/imaging procedures - Brain Imaging

研究概览

简要总结

To characterise phenotypes of Non Proliferative Diabetic Retinopathy (NPDR) progression using multimodal testing/imaging procedures.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Age over 18 years-old.
  • Diabetes mellitus type 2 according to 1985 WHO criteria.
  • Non-proliferative diabetic retinopathy (ETDRS level <= 35)
  • Signs of NPDR progression based on existing clinical information:
  • Retinal thickness (RT) increase (increase in RT above normal range as measured by OCT, considering the macular thickness normative data) in the central subfield, the inner ring and/or the outer ring (leaking phenotype); OR
  • Neovascular disease activity as shown by microaneurysms (MA) turnover (MA formation rate >= 2, i.e. number of new MA per year) computed from CFP using the RetmarkerDR software (ischemic phenotype).
  • Informed consent.

排除标准

  • Cataract or other eye disease that may interfere with fundus examinations
  • Any eye surgery or treatment within a period of 6-months.
  • Pregnant or nursing (lactating) women.
  • Patients with chronic or severe kidney disease (glomerular filtration rate, GFR < 30 mL/min/1.73m2).
  • Patients with acute kidney injury.
  • Patients with known allergic or hypersensitivity reactions to gadolinium, versetamide or any of the inert ingredients.
  • Patients around the time of liver transplantation..
  • Patients with implants containing metals.

结局指标

主要结局

Multimodal testing/imaging procedures - Brain Imaging

时间窗: 12 months

Metabolite concentrations assessed with MR Spectroscopy.

Multimodal testing/imaging procedures - Ophthalmological Imaging

时间窗: 12 months

Blood-Brain Barrier alterations assessed contrast agent with Dynamic MR.

Multimodal testing/imaging procedures - Psychophysical Testing

时间窗: 12 months

Psychophysical tests for speed discrimination, achromatic contrast, and chromatic contrast.

Multimodal testing/imaging procedures - Barin Imaging

时间窗: 12 months

Perfusion change measured with ASL.

次要结局

  • Multimodal testing/ imaging modalities (raw data)(24 months)

研究者

发起方
Association for Innovation and Biomedical Research on Light and Image
申办方类型
Other
责任方
Sponsor

研究点 (1)

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