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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2300069726 |
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最近更新日期: Date of Last Refreshed on: |
2023-05-23 23:25:15 |
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注册时间: Date of Registration: |
2023-03-24 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
多巴胺转运蛋白及脱氧葡萄糖在慢性偏头痛中的临床应用研究 |
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Public title: |
Clinical application of dopamine transporter and deoxyglucose in chronic migraine |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
多巴胺转运蛋白及脱氧葡萄糖在慢性偏头痛中的临床应用研究 |
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Scientific title: |
Clinical application of dopamine transporter and deoxyglucose in chronic migraine |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
常燕 |
研究负责人: |
刘若卓 |
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Applicant: |
Yan Chang |
Study leader: |
Ruozhuo Liu |
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申请注册联系人电话: Applicant telephone: |
+86 18210830630 |
研究负责人电话: Study leader's telephone: |
+86 13910880017 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
1481910234@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
liurz301@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
北京市海淀区复兴路28号 |
研究负责人通讯地址: |
北京市海淀区复兴路28号 |
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Applicant address: |
No. 28 Fuxing Road, Haidian District, Beijing |
Study leader's address: |
No. 28 Fuxing Road, Haidian District, Beijing |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
解放军总医院第一医学中心神经内科 |
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Applicant's institution: |
Department of Neurology Medicine, The First Medical Centre, Chinese PLA General Hospital |
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研究负责人所在单位: |
解放军总医院第一医学中心神经内科 |
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Affiliation of the Leader: |
Department of Neurology Medicine, The First Medical Centre, Chinese PLA General Hospital |
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是否获伦理委员会批准: |
是/Yes |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
S2022-704-01 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
中国人民解放军总医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the Chinese PLA General Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-01-11 00:00:00 |
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伦理委员会联系人: |
曹江 |
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Contact Name of the ethic committee: |
Jiang Cao |
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伦理委员会联系地址: |
北京市海淀区复兴路28号 |
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Contact Address of the ethic committee: |
No. 28 Fuxing Road, Haidian District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
解放军总医院第一医学中心神经内科 |
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Primary sponsor: |
Department of Neurology Medicine, The First Medical Centre, Chinese PLA General Hospital |
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研究实施负责(组长)单位地址: |
北京市海淀区复兴路28号 |
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Primary sponsor's address: |
No. 28 Fuxing Road, Haidian District, Beijing |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
无 |
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Source(s) of funding: |
none |
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Target disease: |
Chronic Migraine |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
II期临床试验 | ||||||||||||||||||||||||||||||||||||||||||||
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Study phase: |
2 |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
本研究利用多巴胺转运蛋白示踪剂 11C-β-CFT 和脱氧葡萄糖示踪剂 18F-FDG 对慢性偏头痛(Chronic migraine, CM)患者进行多参数PET/MR/CT 显像,旨在了解: (1)CM 患者的 11C-β-CFT 分子影像特征。11C-β-CFT 在20 例健康对照人群及20 例CM 患者脑内区域性分布特征。 (2)CM 患者的 18F-FDG 分子影像特征。18F-FDG 在 20 例健康对照人群及 20 例CM 患者 脑内区域性分布特征。 |
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Objectives of Study: |
Multi-parameter PET/MR/CT imaging of a patient with Chronic migraine (CM) using the dopamine transporter tracer 11C-β-CFT and the deoxy-glucose tracer 18F-FDG was conducted in order to understand: (1) Molecular imaging characteristics of 11C-β-CFT in CM patients. Regional distribution of 11C-β-CFT in the brain of 20 healthy controls and 20 CM patients. (2) Molecular imaging features of 18F-FDG in CM patients. 18F-FDG was detected in 20 healthy controls and 20 CM patients Characteristics of regional distribution in brain. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
入组标准:符合国际头痛分类第三版(ICHD-3)中关于慢性偏头痛的诊断标准。入组标准包括:1) 表现为每月头痛超过15d,持续3个月及以上且每月符合偏头痛特点的头痛天数至少8天;2);符合1.1无先兆偏头痛诊断B-D标准和/或1.2有先兆偏头痛B标准和C标准的头痛至少5次;3)主要特征为单侧或双侧交替发作、中重度、搏动性头痛以及劳累后加重为主,通常持续 4~72h,同时可能伴随畏光、畏声、恶心、呕吐等。健康对照组入组标准包括:1) 整体身体状况健康;2) 年龄、性别与实验组患者匹配。 |
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Inclusion criteria |
Inclusion criteria: Met the diagnostic criteria for chronic migraine in the International Classification of Headache, Third Edition (ICHD-3). Inclusion criteria included: 1) Headache manifested as more than 15 days per month, lasted for 3 months or more, and had at least 8 headache days per month consistent with the characteristics of migraine; 2); At least 5 headaches that meet the 1.1 B-D criteria for the diagnosis of migraine without aura and/or 1.2 B and C criteria for migraine with aura; 3) The main characteristics are unilateral or bilateral alternating attacks, moderate and severe, throbbing headache and aggravation after fatigue, usually lasting for 4~72h, and may be accompanied by phobias, phobias, nausea, vomiting, etc. Healthy control group included: 1) overall health status; 2) Age and gender matched with patients in the experimental group. |
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排除标准: |
1)酒精成瘾或药物依赖;2)主要的精神疾病:包括焦虑症,抑郁症,情感障碍,精神分裂症患者,或者药源性精神病等;3) 神经系统疾病:包括脑梗死、脑肿瘤,颅脑外伤等;4) 严重的内科疾病,当前正在使用呼吸系统药物,心血管药物,抗惊厥药物或精神活性物质者;5) 妊娠期、哺乳期妇女及试验期间1个月内计划生育者;6)严重的听觉和视力障碍者;7)入组前预防性服用偏头痛类药物;8) 不能配合随访者。 |
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Exclusion criteria: |
1) Alcohol addiction or drug dependence; 2) Major mental illness: including anxiety disorder, depression, affective disorder, schizophrenia, or drug-induced psychosis; 3) Neurological diseases, including cerebral infarction, brain tumor, craniocerebral trauma, etc. 4) Patients with serious medical conditions who are currently using respiratory drugs, cardiovascular drugs, anticonvulsants or psychoactive substances; 5) Pregnant and lactating women and those who planned to have a family within 1 month during the experiment; 6) People with severe hearing and visual impairment; 7) Prophylactic administration of migraine drugs before enrollment; 8) Can't cooperate with the interviewer. |
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研究实施时间: Study execute time: |
从 From 2023-04-01 00:00:00至 To 2024-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2023-04-01 00:00:00 至 To 2024-12-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
none |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
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盲法: |
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Blinding: |
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是否共享原始数据: IPD sharing |
No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
N/A |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
无 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
N/A |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |