|
注册号: Registration number: |
ChiCTR2500114900 |
|
最近更新日期: Date of Last Refreshed on: |
2025-12-18 16:39:26 |
|
注册时间: Date of Registration: |
2025-12-18 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
老年患者潜在不适当用药及多重用药研究 |
|
Public title: |
Research on Potentially Inappropriate Medication and Polypharmacy in Elderly Patients |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
老年患者潜在不适当用药及多重用药研究 |
|
Scientific title: |
Research on Potentially Inappropriate Medication and Polypharmacy in Elderly Patients |
|
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: |
赵琴琴 |
研究负责人: |
赵琴琴 |
|
Applicant: |
Zhao Qinqin |
Study leader: |
Qinqin Zhao |
|
申请注册联系人电话: Applicant telephone: |
+86 18757152077 |
研究负责人电话:
Study leader's |
+86 571 8997 2240 |
|
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: |
qinqin180@126.com |
研究负责人电子邮件: Study leader's E-mail: |
qinqin180@126.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: |
浙江省杭州市西湖区古翠路234号 |
研究负责人通讯地址: |
浙江省杭州市西湖区古翠路234号 |
|
Applicant address: |
No. 234 Gucui Road, Xihu District, Hangzhou City, Zhejiang Province |
Study leader's address: |
No. 234 Gucui Road, Xihu District, Hangzhou City, Zhejiang Province |
|
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: |
浙江省立同德医院 |
||
|
Applicant's institution: |
Tongde Hospital of Zhejiang Province |
||
|
研究负责人所在单位: |
浙江省立同德医院 |
||
|
Affiliation of the Leader: |
Tongde Hospital of Zhejiang Province |
||
|
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: |
浙同德伦审2025研第465号—JY |
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: |
浙江省立同德医院医学伦理委员会 |
||
|
Name of the ethic committee: |
Medical Ethics Committee of Tongde Hospital of Zhejiang Province |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2025-12-10 00:00:00 | ||
|
伦理委员会联系人: |
朱于青 |
||
|
Contact Name of the ethic committee: |
Zhu YuQing |
||
|
伦理委员会联系地址: |
浙江省杭州市西湖区古翠路234号 |
||
|
Contact Address of the ethic committee: |
No. 234 Gucui Road, Xihu District, Hangzhou City, Zhejiang Province |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 571 89975971 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
zhuyuqingnb@163.com |
|
研究实施负责(组长)单位: |
浙江省立同德医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Tongde Hospital of Zhejiang Province |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
浙江省杭州市西湖区古翠路234号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 234 Gucui Road, Xihu District, Hangzhou City, Zhejiang Province |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
自选课题(自筹) |
||||||||||||||||||||||
|
Source(s) of funding: |
None |
||||||||||||||||||||||
|
研究疾病: |
老年病 |
||||||||||||||||||||||
|
Target disease: |
Geriatric disease |
||||||||||||||||||||||
|
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: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
连续入组 |
||||||||||||||||||||||
|
Study design: |
Sequential |
||||||||||||||||||||||
|
研究目的: |
1.门诊及住院老年患者 PIMs 及多重用药的影响因素分析:收集门诊老年患者处方信息和住院老年患者医嘱信息,并整理患者的人口统计学资料、临床体征、基础疾病情况、医保情况、实验室检查及辅助检查等数据,分析其中可能影响老年患者 PIMs 及多重用药的影响因素。 2.门诊及住院老年患者 PIMs 及多重用药的特征分析:收集并整理老年患者 PIMs 及多重用药情况等。分析老年患者 PIMs 及多重用药的具体药物类型、数量等特征,进一步了解 PIMs及多重用药的特点。 3.门诊及住院老年患者 PIMs 及多重用药的预测模型分析:根据收集到的病例及影响因素,进行数据分析,建立门诊老年患者 PIMs 及多重用药的预测模型,并进行模型验证。 4.亚组分析:针对不同科室或不同疾病的老年患者门诊处方和住院医嘱,开展 PIMs 及多重用药的影响因素、特征及预测模型的亚组分析,包括神经内科、神经外科、老年科、精神科、干保科、康复科、重症医学科、儿科、感染科或其他科室,以及精神疾病患者、躯体疾病伴发抑郁、躯体疾病伴发精神障碍、慢病患者、心脑血管共病患者、泛血管病患者或其他疾病患者的亚组分析。 |
||||||||||||||||||||||
|
Objectives of Study: |
1. Analysis of PIMs and influencing factors of outpatient and inpatient elderly patients: Collect the prescription information of outpatient elderly patients and the doctor's order information of inpatients, and sort out the patient's demographic data, clinical signs, underlying diseases, medical insurance, laboratory examination and auxiliary examination data, and analyze the influencing factors that may affect PIMs and polypharmacy in elderly patients. 2. Characteristic analysis of PIMs and polypharmacy in outpatient and inpatient elderly patients: Collect and sort out PIMs and polypharmacy in elderly patients. The specific drug types and quantities of PIMs and polypharmacy in elderly patients were analyzed to further understand the characteristics of PIMs and polypharmacy. 3. Prediction model analysis of PIMs and polypharmacy in outpatient and inpatient elderly patients: According to the collected cases and influencing factors, the data analysis is carried out, and the prediction model of PIMs and polypharmacy in outpatient elderly patients is established, and the model is verified. 4. Subgroup analysis: Carry out subgroup analysis of PIMs and influencing factors, characteristics and prediction models of PIMs and multiple medications for outpatient prescriptions and inpatient orders of elderly patients with different departments or diseases, including neurology, neurosurgery, geriatrics, psychiatry, cadre nursing, rehabilitation, critical care medicine, pediatrics, infectious diseases or other departments, as well as patients with mental illness, physical diseases with depression, physical diseases with mental disorders, chronic diseases, cardiovascular and cerebrovascular comorbidities, Subgroup analysis of patients with panvascular disease or other diseases. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
1.处方或医嘱信息严重缺失影响统计分析的病例。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1.Cases where the prescription or medical order information is severely incomplete, affecting statistical analysis. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2026-01-01 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-01-01 00:00:00 至 To 2026-12-31 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: |
男女均可 |
Gender: |
Both |
||||||
|
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): |
None |
||||||||
|
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 |
|
盲法: |
无 |
|
Blinding: |
None |
|
是否共享原始数据: IPD sharing |
否No |
|
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 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
N/A |
|
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(CRF) |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |