|
注册号: Registration number: |
ChiCTR2400088671 |
|
最近更新日期: Date of Last Refreshed on: |
2025-11-03 10:40:00 |
|
注册时间: Date of Registration: |
2024-08-23 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
环泊酚和丙泊酚用于重症监护(ICU)患者长时间接受机械通气时镇静的多中心、单盲、 随机对照临床研究 |
|
Public title: |
Cipepofol versus propofol for sdedation in intensive care unit (ICU) patients undergoing long-term mechanical ventilation:a multicenter, single-blind, randomized controlled study. |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
环泊酚和丙泊酚用于重症监护(ICU)患者长时间接受机械通气时镇静的多中心、单盲、 随机对照临床研究方案 |
|
Scientific title: |
Cipepofol versus propofol for sdedation in intensive care unit (ICU) patients undergoing long-term mechanical ventilation:a multicenter, single-blind, randomized controlled 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: |
欧晓峰 |
研究负责人: |
康焰 |
|
Applicant: |
Xiaofeng Ou |
Study leader: |
Yan Kang |
|
申请注册联系人电话: Applicant telephone: |
+86 189 8060 5531 |
研究负责人电话:
Study leader's |
+86 189 8060 1566 |
|
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: |
xiao.ou2006@163.com |
研究负责人电子邮件: Study leader's E-mail: |
kangyan_hx@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: |
四川省成都市武侯区国学巷37号 |
研究负责人通讯地址: |
四川省成都市武侯区国学巷37号 |
|
Applicant address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
Study leader's address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
|
申请注册联系人邮政编码: Applicant postcode: |
610041 |
研究负责人邮政编码: Study leader's postcode: |
610041 |
|
申请人所在单位: |
四川大学华西医院 |
||
|
Applicant's institution: |
West China Hospital, Sichuan University |
||
|
研究负责人所在单位: |
四川大学华西医院 |
||
|
Affiliation of the Leader: |
West China Hospital, Sichuan University |
||
|
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: |
2024年审(1216)号 |
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: |
四川大学华西医院生物医学伦理审查委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of West China Hospital, Sichuan University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2024-08-12 00:00:00 | ||
|
伦理委员会联系人: |
李娜 |
||
|
Contact Name of the ethic committee: |
Na Li |
||
|
伦理委员会联系地址: |
四川省成都市武侯区国学巷37号 |
||
|
Contact Address of the ethic committee: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 8542 2654 |
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: |
四川大学华西医院 |
||||||||||||||||||||||
|
Primary sponsor: |
West China Hospital, Sichuan University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
四川省成都市武侯区国学巷37号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
西藏海思科制药有限公司赞助 |
||||||||||||||||||||||
|
Source(s) of funding: |
Sponsored by Xizang Haisco Pharmaceutical Co., LTD |
||||||||||||||||||||||
|
研究疾病: |
ICU患者镇静 |
||||||||||||||||||||||
|
Target disease: |
Sedation of patients in the ICU |
||||||||||||||||||||||
|
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: |
上市后药物 | ||||||||||||||||||||||
|
Study phase: |
4 |
||||||||||||||||||||||
|
研究设计: |
随机平行对照 |
||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||
|
研究目的: |
主要目的:评价环泊酚用于 ICU 患者接受长时间机械通气时镇静的有效性。 次要目的:评价环泊酚用于 ICU 患者接受长时间机械通气时镇静的安全性和患者预后的影响。 |
||||||||||||||||||||||
|
Objectives of Study: |
Primary Study Objectives: To assess the therapeutic efficacy of Cipepofol for sedation in ICU patients undergoing long-term mechanical ventilation. Secondary Research Objectives: To assess the safety and prognosis of Cipepofol for sedation in ICU patients undergoing long-term mechanical ventilation. |
||||||||||||||||||||||
|
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. 对研究药物禁忌或过敏; 2. 急性严重神经系统疾病和任何其他干扰 RASS 评估的病症 3. 心血管系统疾病:需要药物治疗的心动过缓和/或心率≤50 次/分;II-III 度房室传导阻滞(不包括使用起搏器患者);急慢性心肌炎; 4. 急性肝炎或严重肝功能障碍; 5. 肾小球滤过率 GFR≤30mL/(min*1.73 m2)的慢性肾病患者; 6. 高位截瘫和全身瘫痪患者; 7. 研究者认为血流动力学不可控患者(如适当静脉补液并连续输注 2 种血管升压药后收缩压仍低于 90 mm Hg 患者,休克患者等); 8. 既往有神经类药物及麻醉药物滥用史;筛选期前 3 个月内有酗酒史,长期服用精神类药物等; 9. 妊娠和哺乳期; 10. 筛选前 1 个月内参加其他药物临床试验; 11. 研究者判断患者不适合参加该临床试验的其他情况。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Contraindications or allergies to the study drugs; 2. Acute severe neurological illness and any other conditions that interfere with the RASS assessment; 3. Cardiovascular diseases: bradycardia and/or heart rate ≤ 50 beats/min requiring drug treatment; Degree II-III atrioventricular block (excluding patients with pacemakers); Acute and chronic myocarditis; 4. Acute hepatitis or severe liver dysfunction; 5. Chronic kidney disease patients with glomerular filtration rate GFR ≤ 30 mL/(min * 1.73 m2); 6. Patients with high paraplegia and general paralysis; 7. Patients with uncontrolled hemodynamics (such as patients with systolic blood pressure less than 90 mmHg despite appropriate intravenous fluids and continuous infusion of two vasopressors, or patients with shock, etc.); 8. Previous history of abuse of nerve drugs and narcotic drugs; History of alcohol abuse and long-term use of psychotropic drugs within 3 months before the screening period; 9. Pregnancy and lactation; 10. Participation in other drug clinical trials within 1 month before screening; 11. Any other circumstances in which the patient was judged by the investigator to be ineligible for participation in the trial. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-09-01 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-12-11 00:00:00 至 To 2026-09-01 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: |
正在进行 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): |
签署知情同意书的每例受试者都将获得 5 位数筛选编号,该编号由字母 C+2 位数的研究中心编号和 3 位数字的受试者编号组成。由研究中心按照受试者筛选日期及时间的先后顺序依次发放,一旦发放给受试者后,该筛选编号不能再重复使用。 确定合格的受试者将接受随机化。研究者登录中央随机系统(IWRS)进行随机,获取受试者随机编号和分组信息。 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
Each participant who provided informed consent was assigned a 5-digit screening number composed of the letter C, a 2-digit site number, and a 3-digit subject number. The screening number was issued by the research center based on the date and time of the screening in sequential order. Once the screening number was assigned to the subjects, it could not be reused. Eligible subjects identified will undergo randomization. Investigators logged into the central randomization system (IWRS) for randomization and obtained the randomization number and group information of the subjects. |
||||||||
|
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: |
单盲,受试者盲 |
|
Blinding: |
single-blind, the patients are blinded. |
|
是否共享原始数据: IPD sharing |
是Yes |
|
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): |
临床试验公共管理平台 (http://www.medresman.org.cn/login.aspx) |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
ResMan (http://www.medresman.org.cn/login.aspx) |
|
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 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form (CRF) |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |