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临床试验/NCT03243721
NCT03243721已完成不适用

Impact of Gilenya on Cognitive Function and Thalamic Volume Measured by 7 Tesla MRI in Multiple Sclerosis

The Cleveland Clinic1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2017年10月20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
20
试验地点
1
主要终点
Thalamic volume to cognitive performance

研究概览

简要总结

This evaluation will be a one-year feasibility study to characterize the neuroprotective benefits of Gilenya and its effects on cognition and grey matter volumes. The study will enroll 15 patients with relapsing-remitting multiple sclerosis being treated with Gilenya and 5 healthy controls. Each participant will undergo a battery of neurometric testing at baseline, six months, and one year. In addition, patients will undergo high-field 7T MRI at the same time points.

详细描述

Cognitive impairment is a well-recognized manifestation of multiple sclerosis (MS) with prevalence estimates ranging from 43 to 70%. It is also known to occur as early as the first demyelinating event and is a major factor contributing to quality of life in MS. Treatment strategies for cognitive impairment in MS are limited. Several agents have been tested as therapeutics for MS-related cognitive dysfunction and have showed no major benefit. Cognitive rehabilitation has shown some promise, but the data are limited and many studies have suffered from methodological shortcomings. Given the lack of well-established treatment options and the substantial impact of cognitive impairment, protection of cognitive function from the earliest stages of the disease is of great importance.

Cognitive outcomes received relatively little attention in the pivotal studies of MS disease modifying therapies (DMT), but some data suggest that DMT may have a positive impact on cognition. Gilenya is of special interest because it was found to have a significant protective effect on whole brain atrophy when compared against placebo and intramuscular interferon β-1a in two phase III studies, showing a 31-35% reduction in percentage brain volume change. Gilenya's effect on whole brain atrophy leads to the natural hypothesis that it may have a beneficial effect on cognitive function in MS. Also of particular interest is the extent to which protection of the thalamus and cortex contributes to Gilenya's effect on whole brain atrophy and possible effects on cognition.

The study will enroll 15 subjects from the Cleveland Clinic Mellen Center patient population. Participants must have been on Gilenya for at least 6 months at the time of study entry. The study will involve three assessments: at baseline, six months, and one year. At each time point, participants will undergo 7T MRI of the brain with and without contrast. Participants will also undergo a battery of neurometric testing at each time point. The tests will include the Brief Visuospatial Memory Test - Revised (visuospatial skills), the iPadTM Processing Speed Test (processing speed), the Selective Reminding Test (verbal learning and memory), and the Delis-Kaplan Executive Function System Sorting Test (problem-solving skills; can only be administered at baseline and one year due to version limitations).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

盲法说明

There is no masking in this study.

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •(MS Patients):
  • •RRMS phenotype
  • •Treated with Gilenya for ≥6 months at the time of the baseline visit.
  • •Age 18-50 inclusive.
  • •Disease duration of 5-15 years.
  • •At least 12 years of education (high school diploma or general equivalency diploma).
  • •Physically capable of completing neurometric testing and MRI studies.
  • •Inclusion Criteria (Healthy Controls):
  • •Age 18-50 inclusive.
  • •At least 12 years of education (high school diploma or general equivalency diploma)
  • •Physically capable of completing neurometric testing and MRI studies.

排除标准

  • •(MS Patients):
  • •Contraindication to MRI (e.g. metal implants)
  • •Current use of immunomodulatory or immunosuppressant medications other than Gilenya.
  • •Disease of the central nervous system other than MS (e.g. Alzheimer disease, stroke, epilepsy).
  • •Use of anti-psychotic or psychostimulant medications. Patients started on modafinil or armodafinil more than six months prior to enrollment will not be excluded.
  • •Ongoing major depressive disorder that, in the opinion of the investigator, may affect cognitive functioning.
  • •MS relapse within 90 days of study entry.
  • •Treatment with corticosteroids within 90 days of study entry.
  • •Current illicit substance use.
  • •History of alcohol or drug abuse.
  • •Exclusion Criteria (Healthy Controls):
  • •Contraindication to MRI (e.g. metal implants, claustrophobia).
  • •Disease of the central nervous system (e.g. MS, Alzheimer disease, stroke, epilepsy).
  • •Use of anti-psychotic or psychostimulant medications. Patients started on modafinil or armodafinil more than six months ago will not be excluded.
  • •Ongoing major depressive disorder that, in the opinion of the investigator, may affect cognitive functioning.
  • •Current illicit substance use.
  • •History of alcohol or drug abuse.

研究组 & 干预措施

Gilenya treated MS patients

Experimental

Multiple sclerosis patients treated with Gilenya for at least six months. This group will receive diagnostic tests: 7T MRI and Neurocognitive testing.

干预措施: 7T MRI (Diagnostic Test)

Gilenya treated MS patients

Experimental

Multiple sclerosis patients treated with Gilenya for at least six months. This group will receive diagnostic tests: 7T MRI and Neurocognitive testing.

干预措施: Neurocognitive testing (Diagnostic Test)

Healthy controls

Experimental

Subjects without multiple sclerosis or other diseases of the central nervous system. This group will receive diagnostic tests: 7T MRI and Neurocognitive testing.

干预措施: 7T MRI (Diagnostic Test)

Healthy controls

Experimental

Subjects without multiple sclerosis or other diseases of the central nervous system. This group will receive diagnostic tests: 7T MRI and Neurocognitive testing.

干预措施: Neurocognitive testing (Diagnostic Test)

结局指标

主要结局

Thalamic volume to cognitive performance

时间窗: One year.

Spearman's correlation coefficient of change in thalamic volume and change in cognitive function from baseline to one year in RRMS patients treated with Gilenya.

次要结局

  • Thalamic volume to other MRI metrics(Six months and one year.)
  • Thalamic nuclei to cognitive performance(Six months and one year.)
  • Thalamic myelin density to cognitive performance(Six months and one year.)
  • Thalamic axon density to cognitive performance(Six months and one year.)
  • Changes in MRI metrics in Gilenya treated patients vs. controls(Six months and one year.)
  • Changes in cognitive performance in Gilenya treated patients vs controls(Six months and one year.)
  • Thalamic volume to cognitive performance(Six months.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Devon Conway MD

Principal Investigator

The Cleveland Clinic

研究点 (1)

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