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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: |
ChiCTR2300074906 |
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最近更新日期: Date of Last Refreshed on: |
2023-08-20 05:38:59 |
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注册时间: Date of Registration: |
2023-08-20 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: |
呼气末阻断试验联合肺超声评估神经外科开颅手术患者液体反应性的临床研究 |
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Public title: |
End-expiratory occlusion test combined with lung ultrasound in predicting fluid responsiveness in patients with craniotomy surgery |
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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: |
呼气末阻断试验联合肺超声评估神经外科开颅手术患者液体反应性的临床研究 |
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Scientific title: |
End-expiratory occlusion test combined with lung ultrasound in predicting fluid responsiveness in patients with craniotomy surgery |
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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: |
马宇 |
研究负责人: |
王保国 |
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Applicant: |
Yu Ma |
Study leader: |
Baoguo Wang |
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申请注册联系人电话: Applicant telephone: |
+86 133 6671 8304 |
研究负责人电话: Study leader's telephone: |
+86 133 7018 5075 |
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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: |
1207331159@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
wbgttyy@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: |
北京市海淀区香山一棵松路50号 |
研究负责人通讯地址: |
北京市海淀区香山一棵松路50号 |
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Applicant address: |
No.50,Yikesong Road, Xiangshan, Haidian District, Beijing |
Study leader's address: |
No.50,Yikesong Road, Xiangshan, Haidian District, Beijing |
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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: |
首都医科大学三博脑科医院 |
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Applicant's institution: |
Sanbo Brain Hospital Capital Medical University |
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研究负责人所在单位: |
首都医科大学三博脑科医院 |
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Affiliation of the Leader: |
Sanbo Brain Hospital Capital Medical University |
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是否获伦理委员会批准: |
是/Yes |
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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: |
SBNK-YJ-2023-005-01 |
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: |
首都医科大学三博脑科医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Sanbo Brain Hospital Capital Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-04-09 00:00:00 |
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伦理委员会联系人: |
王鑫 |
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Contact Name of the ethic committee: |
Xin Wang |
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伦理委员会联系地址: |
北京市海淀区香山一棵松路50号 |
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Contact Address of the ethic committee: |
No.50,Yikesong Road, Xiangshan, Haidian District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 6285 6766 |
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: |
首都医科大学三博脑科医院 |
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Primary sponsor: |
Sanbo Brain Hospital Capital Medical University |
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研究实施负责(组长)单位地址: |
北京市海淀区香山一棵松50号 |
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Primary sponsor's address: |
No.50,Yikesong Road, Xiangshan, Haidian District, Beijing |
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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: |
自筹 |
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Source(s) of funding: |
self-financing |
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Target disease: |
patients with craniotomy surgery |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational 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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
主要目的是探讨呼气末阻断实验预测神经外科开颅手术患者液体反应性的可行性及临床价值。次要目的是分析肺超声B线与液体反应之间的关系,观察神经外科开颅患者术后肺部并发症发生情况并分析其危险因素,比较不同液体反应性患者在术后肺部并发症发生情况有无差异。 |
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Objectives of Study: |
The main objective of this study was to investigate the feasibility and clinical value of end-expiratory occlusion test in predicting fluid responsiveness in patients undergoing craniotomy. The secondary objectives were to analyze the relationship between lung ultrasound B-lines and fluid responsiveness, to observe the occurrence of postoperative pulmonary complications in patients undergoing craniotomy and analyze its risk factors, and to compare whether there were differences in the occurrence of postoperative pulmonary complications in patients with different fluid responsiveness. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1)年龄18-70岁; 2)择期行神经外科开颅手术且术后转入重症监护室的患者; 3)手术体位为仰卧位; 4)BMI 17-30kg/m2。 |
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Inclusion criteria |
1) Aged 18-70 years old; 2) patients who underwent elective neurosurgery and were transferred to intensive care unit after surgery; 3) The operation position was supine; 4) BMI 17-30kg/m2. |
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排除标准: |
1)ASA >III级; 2)术前合并肺部感染、放射性肺炎、气胸、皮下气肿、胸腔积液及肺不张、慢 性间质肺疾病伴纤维化病史患者; 3)术前存在未控制的心律失常或已知左心室收缩功能降低(射血分数<50%), 右心室收缩功能下降(三尖瓣环的收缩期峰值速度<0.17ms)。 |
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Exclusion criteria: |
1) ASA >III; 2) preoperative pulmonary infection, radiation pneumonitis, pneumothorax, subcutaneous emphysema, pleural effusion, atelectasis, and slow lung Patients with interstitial lung disease and a history of fibrosis; 3) preoperative uncontrolled arrhythmia or known reduced left ventricular systolic function (ejection fraction <50%); Decreased right ventricular systolic function (peak systolic velocity of the tricuspid annulus <0.17ms). |
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研究实施时间: Study execute time: |
从 From 2023-08-20 00:00:00至 To 2024-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2023-08-20 00:00:00 至 To 2024-06-30 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
No |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
无 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
None |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |