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临床试验/NCT07761026
NCT07761026招募中不适用

AXIS Autoimmune Neurology Registry

Autoimmune Neurology Alliance1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2026年3月19日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
1
主要终点
MG-ADL

研究概览

简要总结

The goal of the AXIS Autoimmune Neurology Registry is to learn about the experiences of adults living with autoimmune neurological disorders, starting with myasthenia gravis (MG), over time.

The main questions the registry aims to answer are:

  • How do symptoms, daily functioning, and quality of life change over time?
  • What treatments do participants use, and how are these treatments related to their symptoms and health?
  • What challenges do participants experience with treatment, including side effects, treatment burden, missed doses, and access to care?

Participants will:

  • Join the registry and complete an enrollment survey (online or through a mobile app)
  • Complete a brief online survey about their MG approximately once a month
  • Provide information that can help confirm their MG diagnosis
  • Optionally, share their medical records with the research team

This is an observational study. The registry will not assign treatments or ask participants to change their medical care. Information collected through the registry may help researchers better understand MG and improve future research and care.

详细描述

The AXIS Autoimmune Neurology Registry is a prospective, longitudinal, observational registry of adults in the United States with autoimmune neurological disorders. The registry is beginning with myasthenia gravis (MG), and participants with MG are currently being enrolled. The registry may expand to include other autoimmune neurological disorders in the future.

The registry is decentralized. Participants complete study activities remotely through a secure website or mobile application. The registry does not assign treatments and does not ask participants to change their usual medical care.

The registry collects information directly from participants to support research on the natural history and real-world management of MG. At enrollment, participants provide information about their MG diagnosis, whether they have ocular or generalized MG, age at diagnosis, demographic characteristics, education, employment, other medical conditions, prior testing, and treatments they have used.

Participants are also asked about MG-related antibody testing, including acetylcholine receptor (AChR), muscle-specific kinase (MuSK), low-density lipoprotein receptor-related protein 4 (LRP4), agrin, and other antibody tests. The registry collects participant-reported information about chest imaging, thymus findings, and thymectomy when applicable.

Participants identify MG treatments they have used and treatments taken during the prior month. These may include symptomatic therapies, corticosteroids, other immunosuppressive therapies, biologic or targeted therapies, intravenous or subcutaneous immunoglobulin, and plasma exchange. Additional questions may collect information about current and prior prednisone doses.

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

  • Physician-confirmed diagnosis of myasthenia gravis (MG)
  • Willing and legally able to provide consent
  • Lives in the United States

排除标准

  • Unwilling or unable to provide consent or comprehend and complete questionnaires
  • Cognitively impaired adults/unable to comprehend or understand the consent or overall study information

研究组 & 干预措施

Myasthenia Gravis (MG)

Adults with confirmed diagnosis of MG

结局指标

主要结局

MG-ADL

时间窗: through study completion, up to 10 years

The Myasthenia Gravis Activities of Daily Living (MG-ADL) profile assesses the severity of myasthenia gravis symptoms during the previous week. Participants rate 8 activities: talking, chewing, swallowing, breathing, brushing teeth or combing hair, rising from a chair, double vision, and eyelid droop. Each item is scored from 0 to 3. Item scores are summed for a total score ranging from 0 to 24. A score of 0 indicates no reported impairment, and higher scores indicate greater symptom severity and functional impairment.

次要结局

  • MG-QOL15r(through study completion, up to 10 years)
  • MGFA Clinical Classification (patient-reported proxy)(through study completion, up to 10 years)

研究者

发起方
Autoimmune Neurology Alliance
申办方类型
Other
责任方
Sponsor

研究点 (1)

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