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注册号: Registration number: |
ChiCTR2100042051 |
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最近更新日期: Date of Last Refreshed on: |
2025-05-26 15:13:13 |
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注册时间: Date of Registration: |
2021-01-13 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: |
前瞻性、多中心、随机对照、非劣效法评价气道冷冻治疗系统的安全性与有效性 |
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Public title: |
A prospective, multi-center, randomized controlled study to evaluate the safety and effectiveness of airway cryotherapy system using non-inferiority method |
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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: |
前瞻性、多中心、随机对照、非劣效法评价气道冷冻治疗系统的安全性与有效性 |
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Scientific title: |
A prospective, multi-center, randomized controlled study to evaluate the safety and effectiveness of airway cryotherapy system using non-inferiority method |
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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: |
黄晨 |
研究负责人: |
宋元林 |
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Applicant: |
Chen Huang |
Study leader: |
Yuanlin Song |
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申请注册联系人电话: Applicant telephone: |
+86 136 7177 8950 |
研究负责人电话:
Study leader's |
+86 150 2175 7762 |
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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: |
huangchen@senscure.net |
研究负责人电子邮件: Study leader's E-mail: |
song.yuanlin@zs-hospital.sh.cn |
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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: |
宁波市杭州湾新区滨海四路777号 |
研究负责人通讯地址: |
上海市徐汇区枫林路180号 |
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Applicant address: |
777 Fourth Binhai Road, Hangzhou Bay New District, Ningbo, Zhejiang |
Study leader's address: |
180 Fenglin Road, Shanghai, China |
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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: |
宁波胜杰康生物科技有限公司 |
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Applicant's institution: |
Ningbo Senscure Biotechnology Co., Ltd. |
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研究负责人所在单位: |
复旦大学附属中山医院 |
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Affiliation of the Leader: |
Zhongshan Hospital, Fudan University |
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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: |
2020-124R |
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: |
复旦大学附属中山医院伦理委员会 |
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Name of the ethic committee: |
Zhongshan Hospital Institutional Review Board |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-11-25 00:00:00 | ||
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伦理委员会联系人: |
李雪宁 |
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Contact Name of the ethic committee: |
Xuening LI |
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伦理委员会联系地址: |
上海市徐汇区枫林路180号 |
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Contact Address of the ethic committee: |
180 Fenglin Road, Shanghai, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 3158 7871 |
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: |
复旦大学附属中山医院 |
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Primary sponsor: |
Zhongshan Hospital, Fudan University |
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研究实施负责(组长)单位地址: |
上海市徐汇区枫林路180号 |
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Primary sponsor's address: |
180 Fenglin Road, Shanghai, 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: |
宁波胜杰康生物科技有限公司 |
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Source(s) of funding: |
Ningbo Senscure Biotechnology Co., Ltd. |
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研究疾病: |
恶性气道狭窄 |
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Target disease: |
Malignant Airway Obstruction |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
评价气道冷冻治疗系统的安全性与有效性。 |
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Objectives of Study: |
To evaluate the safety and effectiveness of the airway cryotherapy system. |
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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. 包含非恶性肿瘤引起的气道狭窄; 2. 伴有外压性狭窄,经研究者评估需要植入支架的患者; 3. 多部位狭窄的患者; 4. 入组前3个月内接受过针对狭窄部位放射治疗的患者; 5. 同期使用EGFR、ALK、ROS1靶向药物治疗的患者(已产生耐药的除外); 6. 狭窄部位气管直径小于4 mm的患者; 7. 存在麻醉、镇静类药物禁忌症; 8. 存在抗凝禁忌或6个月内有出血性疾病发作病史; 9. 严重心律失常、严重器官功能障碍等无法耐受手术治疗的患者; 10. 患有全身感染的患者; 11. 孕期、哺乳期及准备怀孕的女性; 12. 合并其他严重疾病,预期寿命小于3个月者; 13. 入组前3个月内曾参加或正在参加其他药物或器械等临床研究者; 14. 其他经研究者评估不适合纳入本研究的情况,如解剖结构不合适、精神障碍或心理障碍者。 |
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Exclusion criteria: |
1. Airway stenosis induced by non-malignant tumor; 2. External compressive stenosis requiring stent implantation as evaluated by investigators; 3. Stenosis at multiple sites; 4. Having received radiotherapy for the stenosis site within 3 months prior to enrollment; 5. Subjects concurrently receiving EGFR, ALK, and ROS1 targeted therapies (excluding those who have developed resistance); 6. Trachea in a diameter of less than 4 mm at the stenosis site; 7. Contraindications for Anesthetics and Sedatives; 8. Contraindications for anticoagulation therapy or history of hemorrhagic disease within 6 months; 9. Serious arrhythmia, serious organ dysfunction leading to inability to tolerate surgical treatment; 10. Having systemic infection; 11. Pregnant or lactating women as well as those preparing for conception; 12. Combined with other serious diseases with expected lifespan < 3 months; 13. Having participated or participating in other drug or device clinical study within 3 months prior to enrollment; 14. Other conditions evaluated by investigators as unsuitable for inclusion in this study, e.g., unsuitable anatomical structure, mental or psychological disorders. |
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研究实施时间: Study execute time: |
从 From 2021-01-15 00:00:00至 To 2024-02-28 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2021-01-15 00:00:00 至 To 2023-09-30 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: |
结束 /Completed |
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): |
中央系统随机 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Central randomization |
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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: |
开放 |
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Blinding: |
Open-label |
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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): |
研究公开发表后6月内,ResMan 临床试验公共管理平台, http://www.medresman.org.cn |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
ResMan, http://www.medresman.org.cn, within 6 months after the research is publicly published. |
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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: |
EDC, 赛美斯, https://trial.cims-medtech.com/CIMS_V5/?uc=C004 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC, CIMS, https://trial.cims-medtech.com/CIMS_V5/?uc=C004 |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |