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注册号: Registration number: |
ChiCTR2200062370 |
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最近更新日期: Date of Last Refreshed on: |
2023-04-02 18:45:56 |
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注册时间: Date of Registration: |
2022-08-03 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: |
SHR0410 注射液用于择期全身麻醉下行腹腔镜手术后镇痛有效性与安全性研究——多中心、随机、双 盲、安慰剂对照III期临床试验 |
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Public title: |
Efficacy and safety of SHR0410 injection for analgesia after laparoscopic surgery under elective general anesthesia: a multicenter, randomized, double-blind, placebo-controlled phase III clinical trial |
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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: |
SHR0410 注射液用于全身麻醉下行腹腔镜手术后镇痛的有效性与安全性:一项多中心、随机、双盲、安慰剂对照临床研究 |
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Scientific title: |
Efficacy And Safety of SHR0410 Injection for Postoperative Analgesia after Laparoscopic Surgery under General Anesthesia: A Multicenter Randomized, Double-Blind, Placebo-Controlled Clinical Study |
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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: |
周英勇 |
研究负责人: |
欧阳文 |
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Applicant: |
Yingyong Zhou |
Study leader: |
Wen Ouyang |
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申请注册联系人电话: Applicant telephone: |
+86 13787001513 |
研究负责人电话:
Study leader's |
+86 13974934441 |
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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: |
zwyhyll@163.com |
研究负责人电子邮件: Study leader's E-mail: |
ouyangwen133@vip.sina.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: |
湖南省长沙市岳麓区桐梓坡路138号湘雅三医院 |
研究负责人通讯地址: |
湖南省长沙市岳麓区桐梓坡路138号湘雅三医院 |
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Applicant address: |
The Third Xiangya Hospital, 138 Tongzipo Road, Yuelu District, Changsha,Hunan |
Study leader's address: |
The Third Xiangya Hospital, 138 Tongzipo Road, Yuelu District, Changsha,Hunan |
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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: |
中南大学湘雅三医院 |
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Applicant's institution: |
The Third Xiangya Hospital of Central South University |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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是否获伦理委员会批准: |
是 |
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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: |
21247 |
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: |
中南大学湘雅三医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the Third Xiangya Hospital of Central South University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2021-11-23 00:00:00 | ||
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伦理委员会联系人: |
王晓敏 |
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Contact Name of the ethic committee: |
xiaomin wang |
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伦理委员会联系地址: |
湖南省长沙市岳麓区桐梓坡路138号湘雅三医院 |
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Contact Address of the ethic committee: |
The Third Xiangya Hospital, 138 Tongzipo Road, Yuelu District, Changsha,Huna |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
中南大学湘雅三医院 |
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Primary sponsor: |
The Third Xiangya Hospital of Central South University |
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研究实施负责(组长)单位地址: |
湖南省长沙市岳麓区桐梓坡路138号湘雅三医院 |
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Primary sponsor's address: |
The Third Xiangya Hospital, 138 Tongzipo Road, Yuelu District, Changsha,Hunan |
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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: |
江苏恒瑞医药股份有限公司,国家自然科学基金,湖南省自然科学基金,自筹 |
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Source(s) of funding: |
Jiangsu Hengrui Pharmaceutical Co., LTD., National Natural Science Foundation of China, Hunan Natural Science Foundation, Self-funded |
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研究疾病: |
术后疼痛 |
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Target disease: |
Postoperative pain |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
III期临床试验 | ||||||||||||||||||||||
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Study phase: |
3 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
评价SHR0410注射液用于择期全身麻醉下行腹腔镜手术后镇痛的有效性及安全性 |
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Objectives of Study: |
To evaluate the efficacy and safety of SHR0410 injection for postoperative analgesia after laparoscopic surgery under elective general anesthesia. |
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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: |
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Inclusion criteria |
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排除标准: |
1. 筛选前 1 周内有头晕、恶心、干呕、呕吐或合并前庭功能紊乱; |
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Exclusion criteria: |
1. Dizziness, nausea, retching, vomiting or combined vestibular dysfunction within 1 week before screening; |
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研究实施时间: Study execute time: |
从 From 2022-08-01 00:00:00至 To 2023-07-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-08-01 00:00:00 至 To 2023-07-31 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): |
随机编号表和药物编号表由随机化专员利用SAS9.4统计软件产生。采用中央随机化系统进行随机。盲底由随机化专员保管。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Randomization numbering tables and drug-numbering tables were generated by the randomization specialist with the use of SAS9.4 statistical software. Randomization was performed with the use of a central randomization system. The blinds were kept by the randomization specialist. |
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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: |
不公开/Private |
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盲法: |
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Blinding: |
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是否共享原始数据: IPD sharing |
否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(请阅读网站首页注册指南共享原始数据的方式内容) |
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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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |