|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2600126723 |
|
最近更新日期: Date of Last Refreshed on: |
2026-06-15 10:02:31 |
|
注册时间: Date of Registration: |
2026-06-15 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
甲苯磺酸瑞马唑仑用于全麻维持方案与其他全麻方案相比苏醒质量研究 |
|
Public title: |
The study on the recovery quality of remimazolam toluenesulfonate when used as a maintenance anesthetic regimen compared with other anesthetic regimens |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
甲苯磺酸瑞马唑仑用于全身麻醉维持后苏醒时间的观察:一项多中心、双向队列、真实世界研究 |
|
Scientific title: |
Observation of the recovery time after general anesthesia maintenance with remimazolam tosylate: A multicenter, bidirectional cohort, real-world study |
|
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: |
吴先平 |
研究负责人: |
吴先平 |
|
Applicant: |
Xianping Wu |
Study leader: |
Xianping Wu |
|
申请注册联系人电话: Applicant telephone: |
+86 757 25382313 |
研究负责人电话: Study leader's telephone: |
+86 757 25382313 |
|
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: |
sdwxp@163.com |
研究负责人电子邮件: Study leader's E-mail: |
sdwxp@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: |
佛山市顺德区大良金沙大道12号 |
研究负责人通讯地址: |
佛山市顺德区大良金沙大道12号 |
|
Applicant address: |
No.12, Jinsha Avenue, Daliang, Shunde District, Foshan City |
Study leader's address: |
No.12, Jinsha Avenue, Daliang, Shunde District, Foshan City |
|
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: |
广州中医药大学顺德医院 |
||
|
Applicant's institution: |
Shunde Hospital, Guangzhou University of Chinese Medicine |
||
|
研究负责人所在单位: |
广州中医药大学顺德医院 |
||
|
Affiliation of the Leader: |
Shunde Hospital of Guangzhou University of Traditional Chinese Medicine |
||
|
是否获伦理委员会批准: |
是/Yes |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
KY-2025170 |
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: |
广州中医药大学顺德医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of Shunde Hospital of Guangzhou University of traditional Chinese Medicine |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2025-10-15 00:00:00 |
||
|
伦理委员会联系人: |
巫朝银 |
||
|
Contact Name of the ethic committee: |
Wu Chaoyin |
||
|
伦理委员会联系地址: |
佛山市顺德区大良金沙大道12号 |
||
|
Contact Address of the ethic committee: |
No.12, Jinsha Avenue, Daliang, Shunde District, Foshan City |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 757 2232561 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
wuchaoyin1919@163.com |
|
研究实施负责(组长)单位: |
广州中医药大学顺德医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Shunde Hospital of Guangzhou University of Traditional Chinese Medicine |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
佛山市顺德区大良金沙大道12号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No.12, Jinsha Avenue, Daliang, Shunde District, Foshan City |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
广东现代医院管理研究所 |
||||||||||||||||||||||
|
Source(s) of funding: |
Guangdong Institute of Modern Hospital Management |
||||||||||||||||||||||
|
Target disease: |
Patients requiring general anesthesia for surgery. |
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
|
Study phase: |
4 |
||||||||||||||||||||||
|
研究设计: |
队列研究 |
||||||||||||||||||||||
|
Study design: |
Cohort study |
||||||||||||||||||||||
|
研究目的: |
在真实世界中探索在全麻维持阶段使用甲苯磺酸瑞马唑仑对患者苏醒时间的影响。 |
||||||||||||||||||||||
|
Objectives of Study: |
Exploring the effect of remimazolam besylate on emergence time during the maintenance phase of general anesthesia in real-world settings. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1.进行择期手术的患者; 2.美国麻醉医师协会(ASA)分级I~III级; 3.进行全身麻醉患者; 4.前瞻性入组患者知晓本次研究目的并签署知情同意书。 |
||||||||||||||||||||||
|
Inclusion criteria |
1. Patients scheduled for elective surgery; 2. American Society of Anesthesiologists (ASA) physical status classification I to III; 3. Patients undergoing general anesthesia; 4. Prospectively enrolled patients who are informed of the study objectives and provide written informed consent. |
||||||||||||||||||||||
|
排除标准: |
1.对苯?氮?类药物及甲苯磺酸瑞马唑仑成分过敏的患者; 2.重症肌??患者; 3.精神分裂症患者、严重抑郁患者; 4.既往有精神类药物及麻醉药物滥用史患者; 5.既往有癫痫病史或筛选期为癫痫持续状态; 6.孕妇及哺乳期妇女; 7.研究者判断受试者不适合参加本临床研究的情况。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Patients with a known allergy to benzodiazepines or any component of remimazolam besylate; 2. Patients with myasthenia gravis; 3. Patients with schizophrenia or severe depression; 4. Patients with a history of abuse of psychotropic or anesthetic drugs; 5. Patients with a history of epilepsy or in a state of epilepticus at screening; 6. Pregnant or lactating women; 7. Any other condition deemed by the investigator to make the patient unsuitable for participation in this clinical study. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2026-06-01 00:00:00至 To 2028-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2026-06-16 00:00:00 至 To 2028-09-30 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 |
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): |
不共享 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
No sharing. |
|
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: |
由EDC系统记录收集数据 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data is recorded and collected by the EDC system |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |