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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: |
ChiCTR2300068314 |
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最近更新日期: Date of Last Refreshed on: |
2023-02-14 16:36:58 |
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注册时间: Date of Registration: |
2023-02-14 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: |
西维来司他钠治疗轻中度肺源性ARDS的前瞻性、多中心、安慰剂、随机双盲对照临床试验 |
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Public title: |
A prospective, multicenter, placebo, randomized, double-blind controlled clinical trial of cilvelestat sodium in the treatment of mild to moderate pulmonary ARDS |
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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: |
西维来司他钠治疗轻中度肺源性ARDS的前瞻性、多中心、安慰剂、随机双盲对照临床试验 |
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Scientific title: |
A prospective, multicenter, placebo, randomized, double-blind controlled clinical trial of cilvelestat sodium in the treatment of mild to moderate pulmonary ARDS |
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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: |
李娟娟 |
研究负责人: |
詹庆元 |
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Applicant: |
LiJuanjuan |
Study leader: |
ZhanQingyuan |
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申请注册联系人电话: Applicant telephone: |
+86 15662675303 |
研究负责人电话:
Study leader's |
+86 13911785957 |
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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: |
lijuanjuan333@163.com |
研究负责人电子邮件: Study leader's E-mail: |
188870616@qq.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: |
上海市徐汇区东安路562号801室 |
研究负责人通讯地址: |
北京市朝阳区樱花园东街2号 |
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Applicant address: |
Room 801, 562 East 'an Road, Xuhui District, Shanghai |
Study leader's address: |
2 Yinghuayuan East Street, Chaoyang 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: |
上海汇伦江苏药业有限公司 |
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Applicant's institution: |
Shanghai Huilun Jiangsu Pharmaceutical Co. LTD |
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研究负责人所在单位: |
中日友好医院 |
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Affiliation of the Leader: |
China-japan Friendship 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: |
YW2022-051-01 |
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: |
中日友好医院药物(器械)临床试验伦理委员会 |
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Name of the ethic committee: |
China-japan Friendship Hospital Drug (device) Clinical Trial Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-10-26 00:00:00 | ||
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伦理委员会联系人: |
郤思远 |
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Contact Name of the ethic committee: |
XiSiyuan |
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伦理委员会联系地址: |
中日友好医院制剂楼4层415 |
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Contact Address of the ethic committee: |
415, 4th Floor, Pharmaceutical Building, China-Japan Friendship Hospital |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 84206086 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
ZRYHYYGCPEC@126.com |
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研究实施负责(组长)单位: |
中日友好医院 |
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Primary sponsor: |
China-japan friendship Hospital |
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研究实施负责(组长)单位地址: |
北京市朝阳区樱花园东街2号 |
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Primary sponsor's address: |
2 Yinghuayuan East Street, Chaoyang 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: |
上海汇伦江苏药业有限公司 |
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Source(s) of funding: |
Shanghai Huilun Jiangsu Pharmaceutical Co. LTD |
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研究疾病: |
急性呼吸窘迫综合征 |
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Target disease: |
acute respiratory distress syndrome |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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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: |
通过多中心前瞻性随机对照双盲研究,对比西维来司他钠和安慰剂治疗轻中度肺源性ARDS患者对生理指标的改善(氧合指数)、预后和药物安全性。 |
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Objectives of Study: |
A multicenter, prospective, randomized, double-blind study was conducted to compare the improvement of physiological indicators (oxygenation index), prognosis, and drug safety in patients with mild to moderate pulmonary ARDS treated with cilvelestat sodium versus placebo. |
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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: |
(1)年龄≥18岁 |
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Inclusion criteria |
(1) Age ≥18 years old |
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排除标准: |
(1)孕妇,哺乳期妇女 |
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Exclusion criteria: |
(1) Pregnant and lactating women |
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研究实施时间: Study execute time: |
从 From 2023-02-14 00:00:00至 To 2025-01-12 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-02-14 00:00:00 至 To 2025-01-12 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): |
由东南大学统计教研室通过SPASS软件生成随机序列,采用区组随机化的方法 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The random sequence is generated by SPASS software of Statistics Department of Southeast University, The method of block randomization is used. |
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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: |
根据随机信息进行编盲工作,将对试验药物和对照药物进行分类编码、贴签。随机编号为受试者唯一识别码。监查员与研究者必须自始至终处于盲态,编盲过程形成的编盲记录保存。 本试验采用双盲设计,为保证试验过程中盲法的实施,由申办方专门生产外观与试验药物一致的安慰剂,受试对象、药物分发中心工作人员和试验人员均不能根据药物外观判断药物种类。 临床医师负责按纳入标准招募受试对象,按入选先后次序顺次分配随机编号,受试对象姓名和随机编号均由临床医师记录并保存,药品管理员负责药物发放和回收,发放及回收均记录备案,试验揭盲之前,各参与人员均不知道受试对象的分组情况。 |
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Blinding: |
Blinding is carried out based on random information, and the test drugs and control drugs will be classified and labeled. The random number is a unique participant identification number. Supervisors and researchers must be blinded from beginning to end, and the blinding record formed by the blinding process is kept. This trial adopts a double-blind design, in order to ensure the implementation of blinding during the trial, the sponsor specializes in producing placebo with the same appearance as the test drug, and the test subject, the staff of the drug distribution center and the test personnel cannot judge the drug type according to the appearance of the drug. Clinicians are responsible for recruiting subjects according to inclusion criteria, assigning random numbers in order of selection, subject names and random numbers are recorded and saved by clinicians, drug administrators are responsible for drug distribution and collection, distribution and recovery are recorded, and before the trial is unblinded, each participant does not know the grouping of subjects. |
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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): |
德派EDC https://www.nextedc.cn/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
DAPEDC https://www.nextedc.cn/ |
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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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture, EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |