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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: |
ChiCTR2500108190 |
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最近更新日期: Date of Last Refreshed on: |
2025-08-26 16:02:48 |
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注册时间: Date of Registration: |
2025-08-26 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: |
可塑形吸收性骨修复材料治疗腔隙性骨缺损上市后国际多中心、前瞻性、观察性研究 |
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Public title: |
Post-marketing international multicenter, prospective observational study of GaiaBone? Bioabsorbable Bone Graft for the treatment of cavitary bone defects |
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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: |
可塑形吸收性骨修复材料治疗腔隙性骨缺损上市后国际多中心、前瞻性、观察性研究 |
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Scientific title: |
Post-marketing international multicenter, prospective observational study of GaiaBone? Bioabsorbable Bone Graft for the treatment of cavitary bone defects |
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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: |
杨庆诚 |
研究负责人: |
杨庆诚 |
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Applicant: |
Yang Qingcheng |
Study leader: |
Yang Qingcheng |
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申请注册联系人电话: Applicant telephone: |
+86 189 3017 7328 |
研究负责人电话:
Study leader's |
+86 189 3017 7328 |
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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: |
tjyqc@163.com |
研究负责人电子邮件: Study leader's E-mail: |
tjyqc@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: |
中国上海市徐汇区宜山路600号 |
研究负责人通讯地址: |
中国上海市徐汇区宜山路600号 |
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Applicant address: |
No. 600 Yishan Road, Xuhui District, Shanghai, China |
Study leader's address: |
No. 600 Yishan Road, Xuhui District, Shanghai, China |
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申请注册联系人邮政编码: Applicant postcode: |
200233 |
研究负责人邮政编码: Study leader's postcode: |
200233 |
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申请人所在单位: |
上海市第六人民医院 |
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Applicant's institution: |
Shanghai JiaoTong university Affiliated Sixth People‘s Hospital |
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研究负责人所在单位: |
上海市第六人民医院 |
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Affiliation of the Leader: |
Shanghai JiaoTong university Affiliated Sixth People‘s 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: |
2025-KY-210(K)-(1) |
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: |
上海市第六人民医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Shanghai Sixth People‘s Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-08-22 00:00:00 | ||
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伦理委员会联系人: |
庞路阳 |
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Contact Name of the ethic committee: |
Luyang Pang |
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伦理委员会联系地址: |
中国上海市徐汇区宜山路 600 号 |
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Contact Address of the ethic committee: |
No. 600 Yishan Road, Xuhui District, Shanghai, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 6436 9181 |
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: |
上海市第六人民医院 |
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Primary sponsor: |
Shanghai JiaoTong university Affiliated Sixth People‘s Hospital |
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研究实施负责(组长)单位地址: |
中国上海市徐汇区宜山路 600 号 |
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Primary sponsor's address: |
No. 600 Yishan Road, Xuhui District, 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: |
立心(深圳)医疗器械有限公司 |
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Source(s) of funding: |
Corliber (Shenzhen) Medical Device Co., Ltd. |
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研究疾病: |
腔隙性骨缺损 |
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Target disease: |
Lacunar Bone Defect |
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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: |
观察性研究 |
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Study type: |
Observational 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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
对使用了为立心(深圳)医疗器械有限公司生产的可塑形吸收性骨修复材料(该产品已经在六院开展使用)修复腔隙性骨缺损的患者进行真实世界下的前瞻性观察研究,探讨立心(深圳)医疗器械有限公司生产的可塑形吸收性骨修复材料在临床应用中的安全性和有效性。 |
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Objectives of Study: |
A prospective real-world observational study will be conducted on patients with lacunar bone defects repaired using the moldable absorbable bone repair material produced by Lixin (Shenzhen) Medical Devices Co., Ltd. (this product has been used in the Sixth Hospital). The study aims to explore the safety and effectiveness of the moldable absorbable bone repair material manufactured by Lixin (Shenzhen) Medical Devices Co., Ltd. in clinical application. |
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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 18-80 周岁,男性或女性; 2.因各种原因产生腔隙性骨缺损需进行植骨的患者; 3.根据患者自主意愿,拟使用立心(深圳)医疗器械有限公司生产的可塑形吸收性骨修复材料进行骨缺损修复的患者。 4.自愿参加并签署知情同意书、参加临床随访的患者。 5.建议规定各中心作为各自入组患者固定随访点不改动,避免患者流动。 以上五项同时满足方可入选。 |
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Inclusion criteria |
1.Aged 18–80 years, male or female; 2. Patients with lacunar bone defects caused by various reasons who require bone grafting; 3. Patients who, based on their own ,plan to use the moldable absorbable bone repair material produced by Lixin (Shenzhen) Medical Devices Co., Ltd. for bone defect repair; 4. Patients who voluntarily participate in the study, sign the informed consent form, and agree to attend clinical follow-ups; 5. It is recommended that each participating center be designated as a fixed follow-up site for its enrolled patients without changes to avoid patient mobility. Eligibility for enrollment requires meeting all the above five criteria simultaneously. |
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排除标准: |
1.预计依从性差的受试者。 2.患者同时参与了其它临床研究。 3.预计不能按时参加随访的患者。 4.研究者认为其他原因不适合本临床研究者。 若符合以上任意一条,则不能入选 |
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Exclusion criteria: |
1. Subjects expected to have poor compliance. 2. Patients participating in other clinical studies simultaneously. 3.Patients expected to be unable to attend follow-ups on time. 4. Subjects deemed unsuitable for this clinical study by the investigator for other reasons. If any of the above criteria are met, the subject will be excluded from enrollment. |
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研究实施时间: Study execute time: |
从 From 2025-09-01 00:00:00至 To 2027-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-09-25 00:00:00 至 To 2027-04-22 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: |
公开/Public |
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盲法: |
无 |
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Blinding: |
None |
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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 |
否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): |
None |
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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 |
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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 |
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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 |