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临床试验/NCT07526298
NCT07526298尚未招募不适用

Anticipating Irreversible Disability in Neuromyelitis Optica Spectrum Disorder: a Multicenter Prospective Observational Study to Assess Disease Activity in Apparently Stable Patients

IRCCS San Raffaele1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
试验地点
1
主要终点
Identifying predictors of clinical relapse

研究概览

简要总结

The present research is an observational clinical study. The project aims to investigate astrocytic damage, assessed through biological findings such as an increase in GFAP level and/or MRI water index, in patients with NMOSD and its potential role in predicting demyelinating relapses or affecting disability outcomes. It will also explore predictors of astrocytic relapses, focusing on demographic, clinical, and immunological biomarkers like T cell responses, B cell repopulation, and cytokine levels. The goal is to identify unrecognized disease activity, providing insights for future research and clinical trials.

The study will involve 8 sites in Italy: 6 NMOSD clinical centers for patient enrolment and 2 centers for bioengineering and biological analysis. Centralized analysis of the MRI images of all patients enrolled in the clinical centers will be performed by the Neuroimaging Research Unit Fase 1 of San Raffaele Hospital. A total of 50 patients will be included and they will be followed for 12 months.

Comprehensive evaluation of patients, including clinical assessment, bioengineering evaluation, MRI, and blood samples, will be conducted at baseline, month 6, and month 12. To assess silent astrocytic relapses, a specialized evaluation will take place at months 3 and 9, including clinical analysis, blood samples to assess biomarkers like GFAP, a reduced MRI protocol to assess MRI water index, and bioengineering evaluation. In the case of a classical relapse, a dedicated visit will occur within 5 days of symptom onset, using the same evaluation protocol as at months 3 and 9 (MRI and biomarkers will be evaluated if not done in the month before).

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

  • Adult patients (age ≥18 years);
  • NMOSD diagnosis with AQP4 IgG positive status assessed with a cell-based assay;
  • Under rituximab treatment (standard of care) from at least 1 year and for not more than 5 years;
  • Ability to provide written informed consent.

排除标准

  • History of a clinical relapse or new/enlarging T2 lesion during the 6 months preceding the enrollment;
  • Steroids treatment during 30 days before the enrollment;
  • Any contraindication to MRI;
  • Patients currently participating in a different clinical trial;
  • Patients currently pregnant.

研究组 & 干预措施

Adult patients with NMOSD

干预措施: MRI (Diagnostic Test)

Adult patients with NMOSD

干预措施: Immunological Factors (Diagnostic Test)

结局指标

主要结局

Identifying predictors of clinical relapse

时间窗: From enrollment to 12 months

The primary outcomes measures are: percentage of patients with relapse, defined by the occurrence of a novel/worsening NMOSD symptom (detected by patient reported outcomes or clinical judgment or bioengineering indexes) PLUS biological findings of astrocyte damage (increase of GFAP level and/or MRI water index).

次要结局

未报告次要终点

研究者

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

Prof. Massimo Filippi

Prof.

IRCCS San Raffaele

研究点 (1)

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