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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: |
ChiCTR2000039678 |
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最近更新日期: Date of Last Refreshed on: |
2020-11-05 14:41:47 |
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注册时间: Date of Registration: |
2020-11-05 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: |
后颅窝减压术不伴或伴小脑扁桃体电灼对Chiari畸形I型合并脊髓空洞症的疗效评估:一项随机对照试验 |
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Public title: |
Evaluation of Posterior Fossa Decompression (PFD) without or with Cerebellar Tonsil Thermocoagulation (PFDCT) for Arnold-Chiari Malformation Type I with Syringomyelia: a ramdomised controlled trial |
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注册题目简写: |
后颅窝减压术伴小脑扁桃体电灼治疗Chiari畸形I型合并脊髓空洞症随机对照研究 |
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English Acronym: |
PFDCT for Arnold-Chiari Malformation Type I with Syringomyelia |
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研究课题的正式科学名称: |
后颅窝减压术不伴或伴小脑扁桃体电灼对Chiari畸形I型合并脊髓空洞症的疗效评估:一项随机对照试验 |
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Scientific title: |
Evaluation of Posterior Fossa Decompression (PFD) without or with Cerebellar Tonsil Thermocoagulation (PFDCT) for Arnold-Chiari Malformation Type I with Syringomyelia: a ramdomised controlled trial |
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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: |
陈琰 |
研究负责人: |
陈春美 |
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Applicant: |
Chen Yan |
Study leader: |
Chen Chunmei |
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申请注册联系人电话: Applicant telephone: |
13599043836 |
研究负责人电话:
Study leader's |
13509339040 |
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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: |
377260135@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
cmchen2009@sina.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: |
福建省福州市鼓楼区新权路29号 |
研究负责人通讯地址: |
福建省福州市鼓楼区新权路29号 |
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Applicant address: |
No. 29, Xinquan Road, Fuzhou, Fujian, 350001, China |
Study leader's address: |
No. 29, Xinquan Road, Fuzhou, Fujian, 350001, China |
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申请注册联系人邮政编码: Applicant postcode: |
350001 |
研究负责人邮政编码: Study leader's postcode: |
350001 |
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申请人所在单位: |
福建医科大学附属协和医院 |
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Applicant's institution: |
Fujian Medical University Union Hospital |
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研究负责人所在单位: |
福建医科大学附属协和医院 |
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Affiliation of the Leader: |
Fujian Medical University Union Hospital |
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是否获伦理委员会批准: |
是 |
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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: |
2020YF023-01 |
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: |
福建医科大学附属协和医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Affiliated Union Hospital of Fujian Medical University. |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-09-23 00:00:00 | ||
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伦理委员会联系人: |
赖晓玉 |
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Contact Name of the ethic committee: |
Xiao-yu Lai |
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伦理委员会联系地址: |
福建省福州市鼓楼区新权路29号福建医科大学附属协和医院 |
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Contact Address of the ethic committee: |
Fujian Medical University Union Hospital, 29 Xinquan Road, Gulou, Fuzhou, Fujian, China |
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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: |
福建医科大学附属协和医院 |
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Primary sponsor: |
Fujian Medical University Union Hospital |
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研究实施负责(组长)单位地址: |
中国福建省福州市鼓楼区新权路29号 |
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Primary sponsor's address: |
29 Xinquan Road, Gulou, Fuzhou, Fujian, China |
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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: |
福建省临床重点科室经费 |
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Source(s) of funding: |
Funds of Clinical Key Departments of Fujian Province |
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研究疾病: |
Chiari畸形I型合并脊髓空洞症 |
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Target disease: |
Arnold-Chiari Malformation Type I with Syringomyelia |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
治疗新技术临床试验 | ||||||||||||||||||||||
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Study phase: |
New Treatment Measure Clinical Study |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
本文的目的是设计一个多中心、随机、对照临床试验探讨单纯后颅窝去骨瓣减压术相比,后颅窝减压合并小脑扁桃体电灼术的安全性和有效性。 |
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Objectives of Study: |
The purpose of this article is to design a multi-center, randomized, controlled clinical trial to explore the safety and effectiveness of PFDCT compared with PFD. |
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药物成份或治疗方案详述: |
本文的目的是设计一个多中心、随机、对照临床试验探讨单纯后颅窝去骨瓣减压术相比,后颅窝减压合并小脑扁桃体电灼术的安全性和有效性。根据既往研究结果,脱落率设定为 20%,计算样本量为140例。本研究采用分层区组随机的方法,在获得受试者知情同意,并签订知情同意书后,按1:1比例对符合纳入标准的受试者进行随机分组:A 组:施行单纯后颅窝去骨瓣减压(PFD);B 组:施行后颅窝去骨瓣减压合并小脑扁桃体电灼切除术(PFDCT)。本研究采用单盲设计,即随访专员和统计专员采用盲法。但主刀医生、患者和研究助理拥有患者术式及病情知情权。主要结局指标包括:Karnofsky 功能状态评分量表、CCOS 芝加哥 chiari 预后评分、影像学评估空洞变化;次要结局指标包括:疼痛视觉模拟评分、手术相关指标、围手术期的并发症情况。随访时间为术后的1周、1月、3月、6月、12月、24月,合计随访6次。最后采用适当的统计学方法对相关数据进行分析,获得最后的试验结果。 |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
(1)入选年龄:18-65 周岁; |
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Inclusion criteria |
(1) Age: 18-65 years old; |
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排除标准: |
(1)合并有脊柱创伤、神经系统感染性疾病、脊髓肿瘤、脊髓拴系、 后颅窝减压或脊髓疾病手术后等; |
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Exclusion criteria: |
(1) Combined with spinal trauma, nervous system infectious diseases, spinal cord tumors, tethered cord syndrome, posterior fossa decompression or spinal cord disease surgery, etc.; |
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研究实施时间: Study execute time: |
从 From 2021-02-01 00:00:00至 To 2025-02-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2021-02-01 00:00:00 至 To 2023-02-01 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: |
正在进行 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): |
签署书面同意书后,受试者将会按1:1比例随机分配到PFD组或者PFDCT组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Once written informed consent has been obtained, patients are to be randomised to receive either PFD or PFDCT treatment at a ratio of 1:1. |
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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: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
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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: |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |