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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: |
ChiCTR2500099734 |
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最近更新日期: Date of Last Refreshed on: |
2025-03-27 16:47:39 |
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注册时间: Date of Registration: |
2025-03-27 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: |
葡萄糖酸钙锌口服溶液(锌钙特)治疗儿童生长迟缓有效性及安全性的多中心、前瞻性、自身对照的真实世界研究 |
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Public title: |
A multicentre prospective autocontrolled real-world study of the efficacy and safety of calcium and zinc gluconate oral solution (Zinc Calcite) in the treatment of growth retardation in children. |
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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: |
葡萄糖酸钙锌口服溶液(锌钙特)治疗儿童生长迟缓有效性及安全性的多中心、前瞻性、自身对照的真实世界研究 |
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Scientific title: |
A multicentre prospective autocontrolled real-world study of the efficacy and safety of calcium and zinc gluconate oral solution (Zinc Calcite) in the treatment of growth retardation in children. |
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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: |
武欣 |
研究负责人: |
刘振奎 |
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Applicant: |
Wu Xin |
Study leader: |
Liu Zhenkui |
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申请注册联系人电话: Applicant telephone: |
+86 10 8362 4052 |
研究负责人电话:
Study leader's |
+86 313 805 9228 |
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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: |
wuxin@kangzhongshidai.com |
研究负责人电子邮件: Study leader's E-mail: |
liuzhenkui_hb@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: |
北京市丰台区丰科中心A座13层 |
研究负责人通讯地址: |
河北省张家口市桥西区长青路12号 |
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Applicant address: |
13th Floor Block A Fengke Center Fengtai District Beijing |
Study leader's address: |
No.12 Changqing Road Qiaoxi District Zhangjiakou City Hebei Province 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: |
北京康众时代医药科技集团有限公司 |
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Applicant's institution: |
Beijing Kangzhongshidai Pharmaceutical Technology Group Co. Ltd |
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研究负责人所在单位: |
河北北方学院附属第一医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Hebei North 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: |
YJ24-005-04 |
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: |
河北北方学院附属第一医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of The First Affiliated Hospital of Hebei North University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-02-20 00:00:00 | ||
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伦理委员会联系人: |
刘圣君 |
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Contact Name of the ethic committee: |
Liu Shengjun |
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伦理委员会联系地址: |
河北省张家口市桥西区长青路12号 |
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Contact Address of the ethic committee: |
No.12 Changqing Road Qiaoxi District Zhangjiakou City Hebei Province China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 313 805 9228 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
gcpll2019@126.com |
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研究实施负责(组长)单位: |
河北北方学院附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Hebei North University |
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研究实施负责(组长)单位地址: |
河北省张家口市桥西区长青路12号 |
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Primary sponsor's address: |
No.12 Changqing Road Qiaoxi District Zhangjiakou City Hebei Province 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: |
澳诺(中国)制药有限公司 |
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Source(s) of funding: |
Aonuo (China)Pharmaceutical Co.Ltd. |
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研究疾病: |
儿童生长迟缓 |
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Target disease: |
growth retardation in children |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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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: |
探索葡萄糖酸钙锌口服溶液(锌钙特)治疗儿童生长迟缓有效性及安全性。 |
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Objectives of Study: |
To explore the efficacy and safety of calcium and zinc gluconate oral solution (Zinc Calcite) in the treatment of growth retardation in children. |
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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.身高低于同年龄、同性别参照人群值中位数1 SD者; 2.年龄3岁(最小年龄)至10岁(最大年龄)儿童,男女不限; 3.既往未接受生长激素治疗; 4.获得受试儿童/受试者父母/法定监护人签字的知情同意书; 5.受试儿童/受试者父母/法定监护人能够与研究者作良好的沟通。 |
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Inclusion criteria |
1.Persons whose height is less than 1 SD below the median value of the reference population of the same age and sex; 2. Children between the ages of 3 (minimum age) and 10 (maximum age) male and female; 3. No previous growth hormone therapy; 4. Informed consent form signed by the child/subject's parent/legal guardian is obtained; 5. The child/subject's parent/legal guardian is able to communicate well with the investigator. |
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排除标准: |
1.存在影响儿童生长发育的疾病,包括但不限于甲状腺功能异常、甲状旁腺功能异常、生长激素缺乏症、特发性矮小症; 2.存在影响儿童站立或身高测量的疾病,包括但不限于佝偻病、脊柱侧凸、脊柱后凸; 3.存在严重的全身性疾病,如严重心、肺、肝、肾功能不全,严重内分泌系统疾病,严重中枢神经系统和血液疾病; 4.曾接受可能干扰生长激素分泌或生长激素作用的药品治疗; 5.已知或怀疑对研究药品或相关药品过敏者; 6.存在超重的情况,超重以BMI判定:7岁以下儿童的BMI达到+1SD及以上者为超重;7岁以上儿童的BMI大于或等于相应年龄的临界值为超重; 7.研究者判定受试者或父母/法定监护人可能不依从研究实施; 8.研究者认为不适宜纳入者。 |
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Exclusion criteria: |
1. The presence of diseases that affect the growth and development of children including but not limited to abnormal thyroid function abnormal parathyroid function growth hormone deficiency idiopathic dwarfism; 2. The presence of a disease that affects the child's standing or height measurement including but not limited to rickets scoliosis kyphosis; 3. Presence of serious systemic diseases such as severe cardiac pulmonary hepatic and renal insufficiency severe endocrine system diseases severe central nervous system and blood diseases; 4. Previous treatment with drugs that may interfere with growth hormone secretion or growth hormone action; 5. Known or suspected hypersensitivity to the investigational drug or related medications 6. The presence of overweight which was determined by BMI: children under 7 years of age with a BMI of +1SD and above were considered overweight; children over 7 years of age with a BMI greater than or equal to the age-specific threshold were considered overweight; 7. The investigator determines that the subject or parent/legal guardian is likely to be non-compliant with the implementation of the study; 8. Those whom the investigator deems unsuitable for inclusion. |
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研究实施时间: Study execute time: |
从 From 2025-03-26 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-04-01 00:00:00 至 To 2026-04-30 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: |
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: |
不公开/Private |
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盲法: |
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Blinding: |
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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): |
NA |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
NA |
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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: |
eCRF/EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
eCRF/EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |