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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: |
ChiCTR2500097021 |
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最近更新日期: Date of Last Refreshed on: |
2025-02-11 11:08:45 |
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注册时间: Date of Registration: |
2025-02-11 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: |
草乌甲素片治疗慢性肌肉骨骼疼痛前瞻性队列研究 |
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Public title: |
Prospective cohort study on the treatment of chronic musculoskeletal pain with Bulleyaconitine A Tablets |
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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: |
草乌甲素片治疗慢性肌肉骨骼疼痛前瞻性队列研究 |
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Scientific title: |
Prospective cohort study on the treatment of chronic musculoskeletal pain with Bulleyaconitine A Tablets |
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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: |
王宏锴 |
研究负责人: |
陈卫衡/侯志勇 |
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Applicant: |
Wang Hongkai |
Study leader: |
Chen Weiheng/Hou zhiyong |
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申请注册联系人电话: Applicant telephone: |
+86 10 6482 7964 |
研究负责人电话:
Study leader's |
+86 10 5207 5271 |
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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: |
wanghongkai@zyyjypj.cn |
研究负责人电子邮件: Study leader's E-mail: |
drchenweiheng@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: |
北京市昌平区回龙观镇生命科学园路4号 |
研究负责人通讯地址: |
北京市朝阳区安定门外小关街51号/石家庄市友谊北大街102号 |
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Applicant address: |
4 Life Science Park Road, Huilongguan Town, Changping District, Beijing |
Study leader's address: |
No.51 Xiaoguan Street, Andingmen Wai, Chaoyang District, Beijing/No. 102 Youyi North Street, Shijiazhuang City |
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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: |
北京药海宁康医药科技有限公司 |
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Applicant's institution: |
Beijing Yaohai Ningkang Pharmaceutical Technology Co., Ltd. |
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研究负责人所在单位: |
北京中医药大学第三附属医院/河北医科大学第三医院 |
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Affiliation of the Leader: |
The Third Affiliated Hospital of Beijing University of Chinese Medicine/HEBEI MEDICAL UNIVERSITY THIRDHOSPITAL |
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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: |
BZYSY-2024KYKTPJ-47; F2024-017-1 |
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: |
北京中医药大学第三附属医院科研伦理委员会; 河北医科大学第三医院医学伦理委员会 |
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Name of the ethic committee: |
IRB of the Third Hospital Affiliated of Beijing University of Chinese Medicine; Medical Ethics Committee of the Third Hospital of Hebei Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-12-12 00:00:00 | ||
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伦理委员会联系人: |
赵莹 |
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Contact Name of the ethic committee: |
Zhao Ying |
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伦理委员会联系地址: |
北京市朝阳区安定门外小关街51号 |
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Contact Address of the ethic committee: |
No.51 Xiaoguan Street, Andingmen Wai, Chaoyang District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 5207 5242 |
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: |
北京中医药大学第三附属医院/河北医科大学第三医院 |
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Primary sponsor: |
The Third Affiliated Hospital of Beijing University of Chinese Medicine/Hebei Medical University Third Hospital |
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研究实施负责(组长)单位地址: |
北京市朝阳区安定门外小关街51号/石家庄市友谊北大街102号 |
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Primary sponsor's address: |
No.51 Xiaoguan Street, Andingmen Wai, Chaoyang District, Beijing/No. 102 Youyi North Street, Shijiazhuang City |
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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: |
云南昊邦制药有限公司 |
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Source(s) of funding: |
Yunnan Haopy Pharmaceutical Co., Ltd. |
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研究疾病: |
慢性肌肉骨骼疼痛 |
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Target disease: |
Chronic musculoskeletal pain |
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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: |
1.评价草乌甲素片治疗慢性肌肉骨骼疼痛(慢性腰背痛)减轻疼痛、改善机体功能状态等作用的临床效果; 2.分析草乌甲素片治疗慢性肌肉骨骼疼痛(慢性腰背痛)临床效果的异质性(人口统计学差异、疾病分类、不同病因、严重程度、用药方案等); 3.评估临床实际诊疗中草乌甲素片临床应用的安全性; 4.评估临床实际诊疗中草乌甲素片治疗慢性肌肉骨骼疼痛(慢性腰背痛)的经济性。 |
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Objectives of Study: |
1. Evaluate the clinical efficacy of Bulleyaconitine A Tablets in treating chronic musculoskeletal pain (chronic lower back pain), reducing pain, and improving functional status of the body; 2. Analyze the heterogeneity of clinical efficacy of Bulleyaconitine A Tablets in the treatment of chronic musculoskeletal pain (chronic lower back pain) (demographic differences, disease classification, different causes, severity, medication regimen, etc.); 3. Evaluate the safety of clinical application of Bulleyaconitine A Tablets in actual diagnosis and treatment; 4.Evaluate the cost-effectiveness of Bulleyaconitine A Tablets in the treatment of chronic musculoskeletal pain (chronic lower back pain) in clinical practice. |
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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.符合慢性肌肉骨骼疼痛的诊断标准; 2.符合慢性腰背痛的诊断标准; 3.入组前24小时内最痛VAS评分≥4分; 4.年龄≥18岁; |
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Inclusion criteria |
1. Meet the diagnostic criteria for chronic musculoskeletal pain; 2. Meet the diagnostic criteria for chronic lower back pain; 3. The most painful VAS score within 24 hours before enrollment is ≥ 4 points; 4. Age >= 18 years old; |
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排除标准: |
1.除外对草乌甲素片和盐酸度洛西汀肠溶胶囊药物过敏或禁忌证者; 2.孕妇及哺乳期妇女禁用; 3.除外合并严重心脑血管、肝、肾和造血系统、肿瘤等原发性疾病,精神病患者 |
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Exclusion criteria: |
1. Excluding those who are allergic or contraindicated to Bulleyaconitine A Tablets and Duloxetine hydrochloride enteric coated capsules; 2. Pregnant and lactating women are prohibited from using it; 3. Excluding primary diseases such as severe cardiovascular, cerebrovascular, liver, kidney, hematopoietic system, tumors, and psychiatric patients |
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研究实施时间: Study execute time: |
从 From 2025-01-08 00:00:00至 To 2027-02-28 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-02-28 00:00:00 至 To 2026-12-30 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): |
非随机 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
non- randomized |
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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: |
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Blinding: |
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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): |
不适用 |
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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: |
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: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |