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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: |
ChiCTR2300074675 |
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最近更新日期: Date of Last Refreshed on: |
2023-11-15 10:31:23 |
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注册时间: Date of Registration: |
2023-08-11 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: |
靳三针调神针法治疗帕金森病的多中心、随机对照试验 |
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Public title: |
Efficacy of acupuncture (Jin's Three-Needle acupuncture) on Parkinson's disease: a multicenter, prospective, randomized controlled study |
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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: |
靳三针调神针法治疗帕金森病的多中心、随机对照试验 |
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Scientific title: |
Efficacy of acupuncture Jin's Three-Needle acupuncture) on Parkinson's disease: a multicenter, prospective, randomized controlled study |
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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: |
刘鑫 |
研究负责人: |
庄礼兴 |
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Applicant: |
Liu Xin |
Study leader: |
Zhuang Lixing |
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申请注册联系人电话: Applicant telephone: |
+86 135 3488 3118 |
研究负责人电话:
Study leader's |
+86 138 2228 7775 |
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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: |
landy021@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
zhuanglixing@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: |
广东省广州市白云区机场路12号 |
研究负责人通讯地址: |
广东省广州市白云区机场路12号 |
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Applicant address: |
No.12 The airport Road, Baiyun district, Guangzhou, Guangdong |
Study leader's address: |
No.12 The airport Road, Baiyun district, Guangzhou, Guangdong |
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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: |
广州中医药大学第一附属医院 |
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Applicant's institution: |
The First Affiliated Hospital of Guangzhou university of Chinese Medicine |
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研究负责人所在单位: |
广州中医药大学第一附属医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Guangzhou university of Chinese Medicine |
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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: |
K-2023-014 |
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: |
广州中医药大学第一附属医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Guangzhou University of Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-04-26 00:00:00 | ||
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伦理委员会联系人: |
黎欣盈 |
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Contact Name of the ethic committee: |
Li Xinying |
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伦理委员会联系地址: |
广东省广州市白云区机场路12号 |
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Contact Address of the ethic committee: |
No.12 The airport Road, Baiyun district, Guangzhou, Guangdong |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 20 3658 8667 |
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: |
广州中医药大学第一附属医院 |
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Primary sponsor: |
The First Affiliated Hospital of Guangzhou University of Chinese Medicine |
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研究实施负责(组长)单位地址: |
广东省广州市白云区机场路16号 |
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Primary sponsor's address: |
No.16 The airport Road, Baiyun district, Guangzhou, Guangdong |
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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: |
国家自然科学基金 |
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Source(s) of funding: |
Nation Nature Science Foundation of China |
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研究疾病: |
帕金森病焦虑 |
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Target disease: |
Parkinson's disease anxiety |
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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: |
探索性研究/预试验 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Study phase: |
0 |
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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: |
针对帕金森的患者,采用靳三针疗法进行干预,探究靳三针治疗帕金森焦虑及运动症状的临床疗效。 |
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Objectives of Study: |
For patients with Parkinson's disease, the Jin's three-needle acupuncture was used to intervene to explore the clinical efficacy and mechanism of the treatment of Parkinson's disease anxiety and motor symptoms. |
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药物成份或治疗方案详述: |
靳三针组在维持患者原有美多芭剂量的基础上等待4周,结束后予靳三针治疗。等待组在维持患者原有美多芭剂量的基础上等待4周,结束后予靳三针治疗。 |
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Description for medicine or protocol of treatment in detail: |
JTN group:On the basis of maintaining the patient’s original dose of anti-parkinson's drugs, Jin's Three-Needle acupuncture method was given. WL group: On the basis of maintaining the original dose of anti-parkinson's drugs, the patient waited for 4 weeks, and then receivedJin's Three-Needle acupuncture therapy. |
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纳入标准: |
①年龄40-75周岁,男性、女性均可 ②根据2015年国际帕金森病与运动障碍学会的诊断标准,临床诊断确诊为原发性帕金森病 ③Hoehn-Yahr分级为1-3级 ④连续接受抗帕金森药物半年,并接受至少1月稳定剂量的抗帕金森病药物治疗 ⑤能够理解并自愿签署知情同意书 |
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Inclusion criteria |
(1) Meet the criteria of idiopathic PD. (2) Male of female, aged 40 to 75 years old. (3) Hoehn-Yahr staging scale staged 1 to 3. (4) Received anti-parkinsonian drugs for at least 6 months and received stable doses of anti-parkinsonian drugs for at least 1 month. (5) Able to comprehend and willing to sign an Informed Consent Form. |
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排除标准: |
①伴有严重认知功能障碍和幻觉,无法配合量表评价 ②纳入本研究前1个月内曾参加过药物、针灸等其他临床试验者 ③明确有严重的其他系统疾病,如免疫系统疾病、内分泌系统疾病(如嗜铬细胞瘤、甲状腺功能亢进等)、呼吸系统疾病、心脑血管疾病或肝肾功能不全者; ④因不良反应等原因导致无法规律服用抗帕金森药物 ⑤既往或在研究期间计划接受脑深部电刺激疗法或直肠输注左旋多巴治疗的患者 ⑥怀孕或计划怀孕的女性 ⑦正在哺乳期 ⑧有生育计划的受试者 ⑨近半年有某种物质(如酒精、药物、咖啡因)滥用史 ⑩既往有明确精神病史或伴有精神病性症状者; ?害怕针灸者 |
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Exclusion criteria: |
(1) Accompanied by severe cognitive dysfunction and hallucinations, unable to match the scale assessment. (2) Participated in other clinical trials within 1 month. (3) Diagnosed by other severe illness such as heart failure, tumors, renal failure and so on. (4) Unable to regularly take anti-Parkinson's drugs due to adverse reactions or other reasons. (5) Previous or plan to receive deep brain stimulation therapy or levodopa-carbidopa intestinal gel therapy during the study period. (6) Pregnancy or with the intention of pregnancy during the study period. (7) Breastfeeding females. (8) With childbearing potential. (9) Addicted to alcohol or drugs in the past 6 months. (10) Diagnosed by psychotic illness such as schizophrenia, agoraphobia and so on clearly. (11) Afraid of acupuncture. |
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研究实施时间: Study execute time: |
从 From 2023-08-31 00:00:00至 To 2025-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-08-31 00:00:00 至 To 2025-06-30 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): |
采用SPSS Statistics26.0(IBM SPSS Inc.,Chicago,USA)生成随机序列。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
An independent researcher will set a random number as a seed and use IBM SPSS Statistics version 26 (IBM SPSS Inc., Chicago, USA) to generate a random allocation sequence, and each stratum will be generated from this unique random sequence. |
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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: |
本试验采用单盲法,在实施针刺过程中不对医师设盲。仅对结局评价者、统计分析者设盲,即不参加受试者的治疗过程以及不了解受试者的具体分组。 |
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Blinding: |
During the whole trial period, investigators who assess the scales are blinded to the allocation. Assessors who analyze the data are unaware of group assignment either to minimize the potential source of bias. |
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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): |
以论文的形式公布研究结果,需要原始数据的科研工作者可通过邮箱landy021@qq.com获取 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The results will be published by a paper. The original data could be provided by e-mail to scientific researchers who need it. |
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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: |
有/Yes |