|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2400082544 |
|
最近更新日期: Date of Last Refreshed on: |
2024-04-01 08:52:28 |
|
注册时间: Date of Registration: |
2024-04-01 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
评价地舒单抗注射液治疗绝经后脆性骨折患者有效性和安全性的多中心、前瞻性、观察性真实世界研究 |
|
Public title: |
A multicenter, prospective, observational real-world study evaluating the efficacy and safety of Denosumab Injection in the treatment of postmenopausal osteoporotic fractures |
|
注册题目简写: |
地舒单抗真实世界研究 |
|
English Acronym: |
|
|
研究课题的正式科学名称: |
评价地舒单抗注射液治疗绝经后脆性骨折患者有效性和安全性的多中心、前瞻性、观察性真实世界研究 |
|
Scientific title: |
A multicenter, prospective, observational real-world study evaluating the efficacy and safety of Denosumab Injection in the treatment of postmenopausal osteoporotic fractures |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
于海洋 |
研究负责人: |
杨惠林 |
|
Applicant: |
Haiyang Yu |
Study leader: |
Huilin Yang |
|
申请注册联系人电话: Applicant telephone: |
+86 135 9616 0558 |
研究负责人电话:
Study leader's |
+86 139 1263 8099 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
434492855@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
suzhouspine@163.com |
|
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): |
||
|
申请注册联系人通讯地址: |
北京市朝阳区广渠路11号院1号楼金泰国际大厦B805 |
研究负责人通讯地址: |
苏州大学附属第一医院平海路899号 |
|
Applicant address: |
B805, Jintai International Building, Building 1, Yard 11, Guangqu Road, Chaoyang District, Beijing |
Study leader's address: |
The First Affiliated Hospital of Suzhou University, No. 899 Pinghai Road, Suzhou |
|
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: |
||
|
申请人所在单位: |
江苏迈威药业有限公司 |
||
|
Applicant's institution: |
Jiangsu Denko Pharmaceutical Co., Ltd |
||
|
研究负责人所在单位: |
苏州大学附属第一医院 |
||
|
Affiliation of the Leader: |
The First Affiliated Hospital of Suzhou University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
(2024)伦审批第044号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
苏州大学附属第一医院医学伦理委员会伦理审查批件 |
||
|
Name of the ethic committee: |
The First Affiliated Hospital of Suzhou University Medical Ethics Committee ethics review approval |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2024-01-31 00:00:00 | ||
|
伦理委员会联系人: |
陈罡 |
||
|
Contact Name of the ethic committee: |
Gang Chen |
||
|
伦理委员会联系地址: |
江苏省苏州市姑苏区平海路 899 号苏大附一院总院综合楼 1312 办公室 |
||
|
Contact Address of the ethic committee: |
Room 1312, General Hospital, Suzhou University, No. 899 Pinghai Road, Gusu District, Suzhou City, Jiangsu Province |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 512 6797 2861 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
sdfyec@163.com |
|
研究实施负责(组长)单位: |
苏州大学附属第一医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The First Affiliated Hospital of Suzhou University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
苏州市平海路899号苏州大学附属第一医院 |
||||||||||||||||||||||
|
Primary sponsor's address: |
The First Affiliated Hospital of Suzhou University, No. 899 Pinghai Road, Suzhou |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
迈威(上海)生物科技股份有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Provided by Marvelway (Shanghai) Biotech Co., LTD |
||||||||||||||||||||||
|
研究疾病: |
骨质疏松性骨折 |
||||||||||||||||||||||
|
Target disease: |
fragility fracture |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
|
Study phase: |
4 |
||||||||||||||||||||||
|
研究设计: |
连续入组 |
||||||||||||||||||||||
|
Study design: |
Sequential |
||||||||||||||||||||||
|
研究目的: |
观察使用地舒单抗治疗绝经后脆性骨折患者24个月内再骨折的发生率 |
||||||||||||||||||||||
|
Objectives of Study: |
To observe the incidence of refracture within 24 months in patients with postmenopausal fragility fracture treated with sulizumab |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1.绝经后脆性骨折患者。 2.能够符合接受地舒单抗治疗的资格条件。 3.患者及家属充分知情并签署知情同意书。 备注:在进入研究前2周到进入研究后4周内已经开始或将要开始地舒单抗治疗,且同意参加研究的患者,均可参加该研究 |
||||||||||||||||||||||
|
Inclusion criteria |
1.Postmenopausal fragility fracture patients 2.To be eligible for desumab treatment 3.Patients and their families are fully informed and sign informed consent forms remark:Patients who have begun or will begin suzumab treatment within 2 weeks prior to study entry and 4 weeks after study entry, and who agree to participate in the study, may participate in the study |
||||||||||||||||||||||
|
排除标准: |
1.已知对地舒单抗或任何辅料成份过敏者禁用。 2.目前低钙血症。 3.目前维生素 D 严重缺乏(25OHD<10ng/ml)。 4.存在除骨质疏松症以外的骨代谢疾病者: a.各种代谢性骨病,例如骨软化症、成骨不全、佩吉特病等; b.库欣综合征; c.高催乳素血症;d.其他。 5.既往或正患有颌骨骨髓炎或颌骨坏死;牙科手术或口腔手术伤口未愈合;需要口腔手术的急性牙或颌骨病;已计划在研究期间进行有创牙科手术者。 6.5 年内患有恶性肿瘤,或伴有骨转移者,但经治疗后预期可痊愈的肿瘤 (如完全切除的原位皮肤基底细胞或鳞状细胞癌、宫颈癌或乳腺导管癌等) 除外。 7.当前入组在参加其他任何药物研究的患者。 8.研究者认为由于其他原因不适合参加该试验的受试者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. It is prohibited for those who are known to be allergic to desucumab or any excipients. 2. Currently, hypocalcemia. Currently, there is a severe deficiency of vitamin D (25OHD<10ng/ml). 4. Individuals with bone metabolism disorders other than osteoporosis: a. Various metabolic bone diseases, such as osteomalacia, osteogenesis imperfecta, Peggit's disease, etc; b. Cushing's syndrome; c. Hyperprolactinemia; d. Other. 5. Previously or currently suffering from osteomyelitis or necrosis of the jawbone; Dental or oral surgery wounds that have not healed; Acute dental or jaw bone disease requiring oral surgery; Those who have planned to undergo invasive dental surgery during the study period. 6. Patients with malignant tumors or bone metastases within 5 years, except for tumors that are expected to be cured after treatment (such as completely excised in situ basal cell or squamous cell carcinoma of the skin, cervical cancer, or ductal carcinoma of the breast). 7. Patients currently enrolled in any other drug research. 8. The researchers believe that subjects who are not suitable to participate in the trial due to other reasons. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-04-06 00:00:00至 To 2027-04-06 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-04-06 00:00:00 至 To 2027-04-06 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
女性 |
Gender: |
Female |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
NA |
||||||||
|
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 |
|
盲法: |
|
|
Blinding: |
|
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
是Yes |
|
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): |
2027年4月在网站公布https://www.chictr.org.cn/bin/project/edit?pid=220280 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
April 2027 on website https://www.chictr.org.cn/bin/project/edit?pid=220280 |
|
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 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case record fot crf |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |