跳至主要内容
临床试验/NCT03814499
NCT03814499已完成不适用

A Multicentre Longitudinal, Observational Natural History Study to Evaluate Disease Progression in Subjects With Usher Syndrome Type 1B (USH1B)

Fondazione Telethon3 个研究点 分布在 3 个国家目标入组 56 人开始时间: 2018年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
56
试验地点
3
主要终点
BCVA - Better Seeing Eyes

研究概览

简要总结

Natural History Study in Subjects With Usher Syndrome ((USH1B) is a multi-centre, longitudinal, observational study designed to evaluate disease progression in subjects with USH1B by several vision-related assessments.

详细描述

Natural History Study in Subjects With Usher Syndrome (USH1B) is being conducted to understand the progression of disease in USH1B patients as measured by visual acuity and visual field testing and a number of other vision-related assessments. Disease progression will be evaluated as change over time in these measures and associations between the endpoints will be examined.

The primary objective of this study is to evaluate the natural progression of disease over time in USHIB patients using visual field testing and best corrected visual acuity.

The secondary objectives of this study are to evaluate the progression of disease over time in USHIB patients through additional assessments:

  • Microperimetry (only in selected centres)
  • Fundus autofluorescence (FAF)
  • Optical Coherence Tomography (OCT)
  • Full-field Electroretinogram (ERG),
  • Multifocal Electroretinogram,
  • Vision-related function and quality of life, as measured by the 25-Item National Eye Institute Visual Function Questionnaire (NEI VFQ-25)

研究设计

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

入排标准

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

入选标准

  • Must be willing to adhere to protocol for long-term follow-up as evidenced by written informed consent or parental permission and subject assent.
  • Subjects diagnosed with USH
  • Molecular diagnosis of USH1B due to MYO7A mutations (homozygotes or compound heterozygotes).
  • Age eight years old or older at the time of baseline.
  • Visual acuity ≥ 20/640 in at least one eye

排除标准

  • Unable or unwilling to meet requirements of the study.
  • Unable to communicate with suitable verbal/auditory and/or tactile sign language (in the opinion of the investigator)
  • Participation in a clinical study with an investigational drug in the past six months.
  • Pre-existing eye conditions that would interfere with the interpretation of study endpoints (for example, glaucoma, corneal or significant lenticular opacities, cystoid macular oedema, macular hole).
  • Complicating systemic diseases in which the disease itself, or the treatment for the disease, can alter ocular function. Examples are malignancies whose treatment could affect central nervous system function (for example, radiation treatment of the orbit; leukemia with CNS/optic nerve involvement). Also excluded would be subjects with immuno- compromising diseases, as there could be susceptibility to opportunistic infection [such as cytomegalovirus (CMV) retinitis].
  • Subjects with diabetes or sickle cell disease would be excluded if they had any manifestation of advanced retinopathy (e.g. macular edema or proliferative changes).
  • Prior ocular surgery within three months.
  • Any other condition that would not allow the potential subject to complete follow-up examinations during the course of the study and, in the opinion of the investigator, makes the potential subject unsuitable for the study.

结局指标

主要结局

BCVA - Better Seeing Eyes

时间窗: 2 year follow up visit

Change (from Baseline) in Best Corrected Visual acuity (BCVA) in the better-seeing eyes. BCVA in the better seeing eyes was assessed using the ETRS score (minimum value 0 and maximum value 100, with 0 representing the worst, and 100 the best visual functioning). The results are reported as the change in ETDRS score collected at the 2 year follow-up visit compared with the score at the baseline visit.

III4e Area - Better Seeing Eyes

时间窗: 2 year follow up visit

Change (from Baseline) in visual field area using III4e stimulus size in the better seeing eyes. Visual field area using III4e stimulus size in the better seeing eyes is expressed in degree squared (minimum value 0, maximum value 20000). The results are reported as the change in the values collected at the 2 year follow-up visit compared with the values at the baseline visit.

V4e Area - Better Seeing Eyes

时间窗: 2 year follow up visit

Change (from Baseline) in visual field area using V4e stimulus size in the better seeing eyes. Visual field area using V4e stimulus size in the better seeing eyes is expressed in degree squared (minimum value 0, maximum value 20000). The results are reported as the change in the values collected at the 2 year follow-up visit compared with the values at the baseline visit.

BCVA - Worse Seeing Eyes

时间窗: 2 years follow up visit

Change (from Baseline) in Best Corrected Visual acuity in the worse seeing eyes. Best corrected visual acuity in the worse seeing eyes was assessed using the ETRS score (minimum value 0 and maximum value 100, with 0 representing the worst, and 100 the best visual functioning). The results are reported as the change in the ETDRS score collected at the 2 year follow-up visit compared with the score at the baseline visit.

III4e Area - Worse Seeing Eyes

时间窗: 2 years follow up visit

Change (from Baseline) in visual field area using III4e stimulus size in the worse-seeing eyes. Visual field area using III4e stimulus size in the worse-seeing eyes is expressed in degree squared (minimum value 0, maximum value 20000). The results are reported as the change in the values collected at the 2 year follow-up visit compared with the values at the baseline visit.

V4e Area - Worse Seeing Eyes

时间窗: 2 years follow up visit

Change (from Baseline) in visual field area using V4e stimulus size in the worse-seeing eyes. Visual field area using V4e stimulus size in the worse-seeing eyes is expressed in degree squared (minimum value 0, maximum value 20000). The results are reported as the change in the values collected at the 2 year follow-up visit compared with the values at the baseline visit.

次要结局

  • MS - Better Seeing Eyes(2 years follow up visit)
  • CMT - Better Seeing Eyes(2 years follow up visit)
  • EZ Band Horizontal - Better Seeing Eyes(2 years follow up visit)
  • EZ Band Vertical - Better Seeing Eyes(2 years follow up visit)
  • MS - Worse Seeing Eyes(2 years follow up visit)
  • CMT - Worse Seeing Eyes(2 years follow up visit)
  • EZ Band Horizontal - Worse Seeing Eyes(2 years follow up visit)
  • EZ Band Vertical - Worse Seeing Eyes(2 years follow up visit)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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