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临床试验/NCT05229731
NCT05229731撤回不适用

Description of the Neurovisual and Radiological Specificities of Patients With Visual Snow

Fondation Ophtalmologique Adolphe de Rothschild1 个研究点 分布在 1 个国家开始时间: 2022年4月13日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Results of the neurovisual assessment

研究概览

简要总结

NEVICOG is a single-center study evaluating neurovisual and radiological specificities in patients with visual snow syndrome (VSS) compared to a control population.

详细描述

Visual snow syndrome (SNV) is characterized by a continuous grainy or pixelated visual sensation additional to the perceived image. Patients often report a feeling similar to seeing noise from cathode-ray televisions.

The prevalence is not well known but about 2% of the population could be reached. Although benign and stable, this pathology is often troublesome in everyday life.

Its precise etiology remains unknown to this day. Ophthalmologic explorations do not reveal any significant abnormalities. Neurologically, "standard" examinations appear normal. Only the examinations carried out in the context of research have been able to highlight anomalies such as an imbalance between visual cortical inhibition and excitation as well as a high spontaneous neural triggering and hypermetabolism of the associative visual cortex (functional MRI, PET- MRI). In addition, the Visual Evoked Potentials show a lack of habituation, testifying to cortical hyperexcitability.

To our knowledge, no specific neurovisual study focusing on the functions involved in the processing of visual information has been carried out to date. We propose the realization of a complete evaluation made up of existing tasks as well as the adaptation of some of them specific to SNV.

The posterior abnormalities currently highlighted by imaging have been carried out in examinations not available on a daily basis. A non-invasive brain MRI study will be carried out in our patients using more recent techniques (MRI with arterial spin labelling or ASL for Arterial Spin Labelling, and diffusion tensor imaging or DTI for Diffusion Tensor Imaging) in order to search for possible posterior lesions and clinical radiological correlations.

研究设计

研究类型
Observational
观察模型
Case Control
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

  • Case group:
  • Patient aged up to 55
  • Diagnosis of visual snow syndrome according to the international criteria
  • Visual snow symptoms still present
  • Express consent to participate in the study
  • Control group:
  • Person aged up to 60
  • Matched to an SNV patient on age (+/- 5 years) and sex
  • Express consent to participate in the study

排除标准

  • Case group:
  • Patient with an absolute or relative contraindication to MRI (claustrophobia, incompatible implantable device, etc.)
  • Patient benefiting from a legal protection measure
  • Pregnant or breastfeeding woman
  • Non-French speaking patient
  • Added psychiatric or neurodegenerative pathology unrelated to visual snow likely to induce neurocognitive and neurovisual disorders in the short or long term
  • Ophthalmologic comorbidity that may interfere with the interpretation of examinations
  • Control group:
  • Patient with an absolute or relative contraindication to MRI (claustrophobia, incompatible implantable device, etc.)
  • Person benefiting from a legal protection measure
  • Pregnant or breastfeeding woman
  • Non-French speaking person
  • Psychiatric or neurodegenerative pathology likely to induce neurocognitive and neurovisual disorders in the short or long term
  • Ophthalmologic comorbidity that may interfere with the interpretation of examinations

结局指标

主要结局

Results of the neurovisual assessment

时间窗: 1 day (Inclusion)

Rey-Osterrieth test will be used to assess the neurovisual ability. Patients have to reproduce a figure composed of 18 elements. A score between 0 and 2 is given to each of these elements according to their accuracy. The score varies from 0 to 36 and assesses the patient's visuo-constructive ability (36 corresponds to the best visuo-constructive ability).

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

研究点 (1)

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