|
注册号: Registration number: |
ChiCTR2300077426 |
|
最近更新日期: Date of Last Refreshed on: |
2024-05-27 14:41:10 |
|
注册时间: Date of Registration: |
2023-11-08 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
0.5%罗哌卡因用于超声引导股神经阻滞的90%最小有效容积:有偏硬币序贯法 |
|
Public title: |
The 90% minimum effective volume of 0.5 ropivacaine for ultrasound-guided femoral nerve block: A biased coin up-and-down design |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
0.5%罗哌卡因用于超声引导股神经阻滞的90%最小有效容积:有偏硬币序贯法 |
|
Scientific title: |
The 90% minimum effective volume of 0.5 ropivacaine for ultrasound-guided femoral nerve block: A biased coin up-and-down design |
|
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: |
轩庆航 |
研究负责人: |
彭婧 |
|
Applicant: |
Qinghang Xuan |
Study leader: |
Peng Jing |
|
申请注册联系人电话: Applicant telephone: |
+86 152 5306 6603 |
研究负责人电话:
Study leader's |
+86 198 6183 0953 |
|
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: |
xuanqinghang@163.com |
研究负责人电子邮件: Study leader's E-mail: |
xuanqinghang@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: |
云南省大理市嘉士伯大道32号 |
研究负责人通讯地址: |
云南省大理市嘉士伯大道32号 |
|
Applicant address: |
32 Garsberg Road, Dali, Yunnan |
Study leader's address: |
32 Garsberg Road, Dali, Yunnan |
|
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: |
云南省大理市大理大学第一附属医院 |
||
|
Applicant's institution: |
The First Affiliated Hospital of Dali University, Dali, Yunnan |
||
|
研究负责人所在单位: |
云南省大理市大理大学第一附属医院 |
||
|
Affiliation of the Leader: |
The First Affiliated Hospital of Dali University, Dali, Yunnan |
||
|
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: |
DFY20230926001 |
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: |
大理大学第一附属医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Dali University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2023-09-26 00:00:00 | ||
|
伦理委员会联系人: |
路会霞 |
||
|
Contact Name of the ethic committee: |
Huixia Lu |
||
|
伦理委员会联系地址: |
云南省大理市嘉士伯大道32号 |
||
|
Contact Address of the ethic committee: |
32 Garsberg Road, Dali, Yunnan |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 872 220 1096 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
|
|
研究实施负责(组长)单位: |
大理大学第一附属医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The First Affiliated Hospital of Dali University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
云南省大理市嘉士伯大道32号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
32 Garsberg Road, Dali, Yunnan |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
研究者自费 |
||||||||||||||||||||||
|
Source(s) of funding: |
Investigator's expense |
||||||||||||||||||||||
|
研究疾病: |
神经阻滞 |
||||||||||||||||||||||
|
Target disease: |
Nerve block |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
干预性研究 |
||||||||||||||||||||||
|
Study type: |
Interventional study |
||||||||||||||||||||||
|
研究所处阶段: |
治疗新技术临床试验 | ||||||||||||||||||||||
|
Study phase: |
New Treatment Measure Clinical Study |
||||||||||||||||||||||
|
研究设计: |
单臂 |
||||||||||||||||||||||
|
Study design: |
Single arm |
||||||||||||||||||||||
|
研究目的: |
通过我们对股神经横截面积(CSA)的研究,减少局麻剂量,提高麻醉的安全性。 |
||||||||||||||||||||||
|
Objectives of Study: |
Through our study on the cross-sectional area(CSA) of the sfemoral nerve, the dose of local anesthesia can be reduced and the safety of anesthesia can be improved. |
||||||||||||||||||||||
|
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.拒绝参加研究; 2.妊娠及哺乳期; 3.局部麻醉药过敏史; 4.神经和精神系统疾病; 5.糖尿病史; 6.凝血功能障碍; 7.酗酒史; 8.沟通障碍; 9.2周内使用阿片类药物或非甾体药物; 10.局部麻醉药扩散不佳。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Refusal to participate in the study; 2. Pregnancy and lactation; 3. History of allergy to local anesthetics; 4. Neurological and psychiatric disorders; 5. History of diabetes; 6. Coagulation disorders; 7. History of alcoholism; 8. Communication barriers; 9. Use of opioids or nonsteroidal drugs within 9.2 weeks; 10. Poor diffusion of local anesthetics. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2023-11-15 00:00:00至 To 2023-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-11-15 00:00:00 至 To 2023-12-31 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): |
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 |
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): |
NA |
|
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): 研究信息: 研究名称: 研究设计: 研究目的: 患者基本信息: 姓名: 年龄: 性别: 民族: 联系方式: 临床特征和诊断信息: 症状描述: 诊断结果: 入选标准是否满足: 排除标准是否存在: 治疗信息: 治疗方案: 药物名称和剂量: 给药途径: 观察指标和终点: 观察指标定义: 观察指标记录: 终点事件发生情况: 不良事件记录: 不良事件描述: 不良事件严重程度: 不良事件处理措施: 电子数据采集和管理系统(EDC): 试验信息输入: 患者基本信息输入情况: 治疗信息输入情况: 观察指标输入情况: 数据验证和审核: 数据验证情况报告: 数据审核结果记录: 数据安全措施: 数据加密情况: 访问控制措施: 数据备份频率: 数据备份和维护: 数据备份情况报告: 系统维护记录: |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form (CRF): Study Information: Study Name: Study Design: Study Purpose: Patient Basic Information: Name: Age: Gender: Ethnicity: Contact Information: Clinical Characteristics and Diagnosis Information: Symptom Description: Diagnosis Result: Fulfillment of Inclusion Criteria: Existence of Exclusion Criteria: Treatment Information: Treatment Plan: Name and Dosage of Medication: Route and Frequency of Administration: Observation Indicators and Endpoints: Definition of Observation Indicators: Record of Observation Indicators: Occurrence of Endpoint Events: Adverse Event Records: Description of Adverse Events: Severity of Adverse Events: Measures for Dealing with Adverse Events: Electronic Data Capture and Management System (EDC): Entry of Trial Information: Status of Patient Basic Information Entry: Status of Treatment Information Entry: Status of Observation Indicators Entry: Data Validation and Review: Data Validation Report: Record of Data Review Results: Data Security Measures: Data Encryption Status: Access Control Measures: Data Backup Frequency: Data Backup and Maintenance: Data Backup Report: System Maintenance Record: |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |