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注册号: Registration number: |
ChiCTR1900024635 |
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最近更新日期: Date of Last Refreshed on: |
2019-07-19 16:42:30 |
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注册时间: Date of Registration: |
2019-07-19 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
评价药物洗脱球囊导管与紫杉醇释放冠脉球囊导管 SeQuent Please治疗冠状动脉支架内再狭窄病变患者的安全性和有效性的前瞻性、多中心、随机对照临床试验 |
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Public title: |
Prospective, multicenter, randomized controlled clinical trial to evaluate the safety and efficacy of a drug-eluting balloon catheter, and SeQuent Please for patients with coronary stent restenosis |
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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: |
评价药物洗脱球囊导管与紫杉醇释放冠脉球囊导管 SeQuent Please治疗冠状动脉支架内再狭窄病变患者的安全性和有效性的前瞻性、多中心、随机对照临床试验? |
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Scientific title: |
Prospective, multicenter, randomized controlled clinical trial to evaluate the safety and efficacy of a drug-eluting balloon catheter, and SeQuent Please for patients with coronary stent restenosis |
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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: |
张羽 |
研究负责人: |
胡玺 |
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Applicant: |
Yu Zhang |
Study leader: |
Xi Hu |
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申请注册联系人电话: Applicant telephone: |
+86 15221259151 |
研究负责人电话:
Study leader's |
+86 13817021433 |
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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: |
yzhang@heart-acme.com |
研究负责人电子邮件: Study leader's E-mail: |
xhu@heart-acme.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: |
上海市浦东新区张江高科技东区瑞庆路590号9幢北302室 |
研究负责人通讯地址: |
上海市浦东新区张江高科技东区瑞庆路590号6幢乙301室 |
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Applicant address: |
Suite 302, Building 9, 590 Ruiqing Road, East Zhangjiang High-Tech Park, Shanghai, China |
Study leader's address: |
Suite 301, Building 6, 590 Ruiqing Road, East Zhangjiang High-Tech Park, Shanghai, China |
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申请注册联系人邮政编码: Applicant postcode: |
201201 |
研究负责人邮政编码: Study leader's postcode: |
201201 |
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申请人所在单位: |
上海安通医疗科技有限公司 |
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Applicant's institution: |
Shanghai Angiocare Medical Technology Co.,Ltd |
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研究负责人所在单位: |
上海安通医疗科技有限公司 |
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Affiliation of the Leader: |
Shanghai Angiocare Medical Technology Co.,Ltd |
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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: |
2018伦审械临字第(9)号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
太原市中心医院药物临床试验机构伦理委员会 |
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Name of the ethic committee: |
Ethics committee of drug clinical trial institution of taiyuan central hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2018-07-27 00:00:00 | ||
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伦理委员会联系人: |
芦云 |
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Contact Name of the ethic committee: |
Yun Lu |
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伦理委员会联系地址: |
山西省太原市解放北路东二道巷7号(太原市中心医院办公楼703室) |
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Contact Address of the ethic committee: |
Room 703, Office Building, Central Hospital, Taiyuan, Shanxi, 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: |
空军军医大学西京医院 |
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Primary sponsor: |
Xijing Hospital, Military Medical University of The Air Force |
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研究实施负责(组长)单位地址: |
陕西省西安市长乐西路15号 |
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Primary sponsor's address: |
15 West Changle Road, Xi'an, Shaanxi, 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: |
自然人投资 |
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Source(s) of funding: |
Natural person investment |
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研究疾病: |
冠状动脉支架内再狭窄 |
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Target disease: |
Coronary stent restenosis |
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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: |
III期临床试验 | ||||||||||||||||||||||
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Study phase: |
3 |
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研究设计: |
随机交叉对照 |
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Study design: |
Cross-over |
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研究目的: |
验证上海心至医疗科技有限公司生产的药物洗脱球囊导管在冠状动脉支架内再狭窄患者中临床使用的安全性及有效性。 |
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Objectives of Study: |
To verify the safety and efficacy of drug-eluting balloon catheter in patients with coronary stent restenosis produced by Shanghai xinzhi medical technology co., LTD |
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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: |
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Inclusion criteria |
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排除标准: |
1.处于妊娠或哺乳期女性,或未来一年内有生育计划者; |
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Exclusion criteria: |
1. Women who are pregnant or breast-feeding, or have family planning within the next year; |
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研究实施时间: Study execute time: |
从 From 2018-08-01 00:00:00至 To 2020-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2018-10-01 00:00:00 至 To 2019-10-31 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: |
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): |
本研究为随机对照临床试验,试验将采取基于计算机系统的中央随机法,当有病人符合试验入选/排除标准、签署了知情同意书需要随机时,研究者再登陆随机网站进行随机,计算机系统将根据患者情况自动分配随机号及相应的治疗组别,在获得随机结果后,研究者应根据系统分配的组别对患者进行治疗。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This study for randomized, controlled clinical trials, the test will take the central stochastic method based on computer system. |
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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: |
未说明 |
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Blinding: |
Not stated |
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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): |
取得产品注册证后公开;临床试验公共管理平台ResMan (www.medresman.org) |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Plan to release the original data after obtaining the product registration certificate;ResMan (www.medresman.org) |
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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: |
病例记录表和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: |
Case Record Form and Electronic Data Capture |
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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 |