China clinical trial registry. CTRI Clinical Trials Registry India [Internet].

China clinical trial registry Clinical research in China is regulated and overseen by the National Medical Products Administration (NMPA) (the Chinese name translates as “State Drug Administration”) and th 中国临床试验注册中心（China Clinical Trial Registry，简称 CCTR）是我国临床试验注册的官方机构，负责我国临床试验的注册管理工作。CCTR 旨在推动我国临床试验的科学、规范和国际化发展，为公众、研究者、企业和政府提供临床试验信息服务。 中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）是由四川大学华西医院吴泰相教授和李幼平教授团队于2005年建立、2007年由卫生部指定其代表我国参加世界卫生组织国际临床试验注册平台的国家临床试验注册中心，并于同年被认证为世界卫生组织国际临床试验注册平台的一级注册机构，是非 Objective: This research aims to examine the basic and methodological characteristics of anticancer drug studies registered on the Chinese Clinical Trial Registry (ChiCTR) and explores the progress of implementation of good clinical practice (GCP) and the challenges it poses for anticancer drug research in China. CMUH has been a trusted collaborative partner for many global pharmaceutical companies and contract research organizations (CROs). Search for terms 1 Introduction. For any updates to trial information, you can use the China Clinical Trial Registry (ChiCTR) directly at https://www. Location. Methods: A multi-dimensional grouping analysis was conducted to estimate trends in annual trial registration, China's clinical trial registry is called ChiCTR: chictr. Modify the protocol, suspend or terminate the clinical trial as needed, and report to the Center for Drug Evaluation (CDE) if safety issues or other risks are identified during a clinical trial, in a timely fashion Summary of clinical trial register in China • 至2009年11月20日 已注册588个临床试 验，其中260个为政 府支持项目 • 588 clinical trials have been registered until Nov. 1,137. The ICTRP Search Portal aims to provide a single point of access to information about ongoing and completed clinical trials. 0 or later 从网站页面的简介来看，中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）是由卫生部指定代表我国参加世界卫生组织国际临床试验注册平台的国家临床试验注册中心；是世界卫生组织国际临床试验注册平台的一级注册机 Glossary. 中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）是由卫生部指定代表我国参加. From which countries will the Registry accept trials for registration? All countries. Taichung City. [2] Cuba. It accepts prospective r Relevant researches can be registered on the International Traditional Medicine Clinical Trial Registry (ITMCTR, http://itmctr. Not applicable. (from website) Prefix chictr Links Q15: According to the Decisions on Affairs relevant to Adjusting the Administration of Imported Drug Registration (former CFDI's No. Our clinical trial partners include the world’s top 50 international pharmaceutical companies. 0 or later The mission of the WHO International Clinical Trials Registry Platform is to ensure that a complete view of research is accessible to all those involved in health care decision making. doctors/PIs. As well as interventional studies the register also includes prevention studies, diagnostic test studies, prognostic studies and epidemiological research. It provides a searchable database containing the trial registration data sets made available by data providers around the world meeting criteria for content and quality control. It is supported by secondary institutions like the Chinese University of Hong Kong Clinical Trials Registry and the Traditional Chinese Medicine Clinical Trials Registry. It was established in October 2005. Earlier this year, we reported technical difficulties in accessing results on the Chinese Clinical Trial Registry in a presentation at the REWARD– EQUATOR 2020 conference, as part of our ongoing work examining clinical trial registries. Keywords: Advanced solid tumors; Combination anti-TIGIT and anti-PD-L1 cancer immunotherapy; Ethnic sensitivity and population bridging; Immune check point inhibitors; Phase I clinical trials. cn. 蜀ICP备16010396号-9. Fifteen key items were analysed to describe trial characteristics, CTRI Clinical Trials Registry India [Internet]. However, you will still be able to view the existing registration details. 0 or later To date, a large number of clinical trials addressing various aspects of COVID-19 have been registered in the Chinese Clinical Trial Registry (ChiCTR), including more than 200 interventional studies. 0 or later Chinese Clinical Trial Registry (ChiCTR) Profile Website : Clinical Research Information Service (CRiS), Republic of Korea Profile International Traditional Medicine Clinical Trial Registry (ITMCTR) Profile (updated on 29-03-2022) Website: Japan Registry of Clinical Trials (jRCT) Profile (updated on 26-10-2023) Trial search Nation, Province(City) Code of disease Primary sponsor(s) Secondary sponsor(s) Funding source Recruiting status Register status Measure Ethical committee Study type A Multi-Center Single-Blind, Randomized, Controlled Trial Evaluating the SARS-CoV-2 Rebound rate after full-course treatment of JT001 (VV116) Compared to Paxlovid for the Early Treatment of The other primary registries, namely Australian New Zealand Clinical Trials Registry (ANZCTR), Brazilian Clinical Trials Registry (ReBec), Chinese Clinical Trial Registry (ChiCTR), Clinical Research Information Service (CRiS), Republic of Korea, Clinical Trial Registry India (CTRI), Cuban Public Registry of Clinical Trials (RPCEC), EU Clinical Trials Register (EU‑CTR), Since registries are similar in many ways to clinical trials, simple protocol that will provide guidance on the different safety requirements that exist for a registry—not a clinical trial—and then facilitate the regulatory team in Paediatric drug trials in China made a significant progress in recent years. Global registry China's clinical trial registry is called ChiCTR: chictr. The DRR authorizes regulatory pathways for priority review and approval (including for breakthrough therapeutic drugs), conditional Database allows English or Chinese search options. HKU Clinical Trials Registry (HKUCTR) is a public online registry established at the Clinical Trials Centre, The University of Hong Kong (HKU-CTC) in June 2005, with management support from the Li Ka Shing Faculty of Medicine, The University of Hong Kong. To date, a large number of clinical trials addressing various aspects of COVID19 have been registered in the Chinese Clinical Trial Registry (ChiCTR), including more than 200 interventional studies. Search for terms Clinical Trial Center, China Medical University Hospital. As well as interventional studies the register also includes Following the 2004 declaration by the International Committee of Medical Journal Editors (ICMJE), which mandated that ICMJE member journals only publish results of clinical trials As a national public clinical trial registry and a recognized Primary Registry of the WHO ICTRP, the Chinese Clinical Trial Registry (ChiCTR) has responsibility to disseminate knowledge The Chinese Clinical Trial Registry (ChiCTR, http://www. CMUH has been a trusted collaborative partner for many global pharmaceutical companies and contract research As a national public clinical trial registry and a recognized Primary Registry of the WHO ICTRP, the Chinese Clinical Trial Registry (ChiCTR) has responsibility to disseminate knowledge about clinical trial transparency, which is an important ethical issue for healthcare studies involving humans, and to promote the quality of healthcare studies in China. National Medical Products Administration. gov and Chinese Clinical Trial Registry databases in 22 April 2019. The DRR clarifies that the NMPA 2. Trial registration data sets are available on the Chinese Clinical Trial Registry. Database allows English or Chinese search options. Purpose and significance In order to comprehensively master the current situation of clinical trials of new drug registration in China, promptly disclose the information on the progress of clinical trials, and provide Chinese Clinical Trial Registry. Objective: The objective of this study is to describe the profile of all the primary registries including Clinical Trial Registry‑India (CTRI), through features such as magnitude, domain of 中国临床试验注册中心（Chinese Clinical TrialRegistry，ChiCTR）是由卫生部指定代表我国参加世界卫生组织国际临床试验注册平台的国家临床试验注册中心，是世界卫生组织国际临床试验注册平台的一级注册机构，签署《渥太华工作组关于临床试验注册的声明》(Ottawa Group Statement for Clinical Trial Registration 国际医学期刊编辑委员会要求：前瞻性临床研究均需在纳入第一名受试者前进行临床研究注册，可在以下网址进行注册： Chinese Clinical Trial Registry: mission, responsibility and operation Taixiang Wu, Youping Li∗, Guanjian Liu, Jing Li, Li Wang, Liang Du, on behalf of the Chinese Clinical Registry Chinese Clinical Registry, Chinese Cochrane Centre, Chinese Evidence-Based Medicine Centre, INCLEN CERTC, West China Hospital, Sichuan University, Chengdu 610041 The Chinese scientists supported by private and government resources have adopted extensive efforts to identify effective drugs against the virus. beds. It participates in the WHO's ICTRP. So Overview. The advanced retrieval function is used to retrieve clinical trials data in the Clinical Trial. 1 The Centre for Clinical Research and Biostatistics – Clinical Trials Registry (CCRBCTR), provides all prospective registrants with a convenient means to submit trial registration for all countries. . New Delhi: database publisher (India). Setting Registration information registered prior to 31 December 2018 was obtained EU-CTR, EU Clinical Trials Register. Clinical Trials For registered clinical trials to support a marketing application, it is recommended that they be completed before the marketing application To achieve some kind of commitment, recognition or contract through sex. As The Chinese Clinical Trial Registry (ChiCTR) is a national clinical trial registry designated by the Ministry of Health (MOH) to represent China in the World Health Organization International ICTRP Search Portal. In accordance with the DRR, the DAL, the NMPA-No50-2018, the SC-Opinions-No44, and the NMPA-No230-2015, the National Medical Products Administration (NMPA) is responsible for reviewing and approving clinical trial applications for drugs to be registered in China, as required. Identifier CTRI/2008/091/000052, A clinical trial to study the effects of Ayurvedic formulation containing Ashwagandha and Guduchi in improving the quality of Registrants who wish to register clinical trials in TCTR are obliged to disclose details of the 24 mandatory items of the WHO International Clinical Trials Registry Platform (WHO-ICTRP) dataset. 1. 有关新系统使用方法和填写要求，网页打开、信息保存、提交、上传附件失败，账户对接后品种、试验丢失等问题，请先查阅“登记常见问题”栏目查阅解决方法。 Expedited Clinical Trial Review. 世界卫生组织国际临床试验注册平台的国家临床试验注册中心； 是世界卫生组织国际临床试验注册平台的一级注册机构，是一个非赢利的学术机构。 The mission of ChiCTR is to “unite clinicians, clinical epidemiologists, biostatisticians, epidemiologists and healthcare managers both at home and abroad, to manage clinical trials in a strict and scientific manner, and to promote their quality in China, so as to provide reliable evidence from clinical trials for health care workers, consumers and medical policy decision org) has been assigned as the national clinical trial registry for China, is part of the World Health Organization’s Inter-national Clinical Trial Registry Platform (WHO ICTRP) and was recognized as a Primary Registry of ICTRP in 2007 (1). This will improve research transparency and will ultimately 中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）于2005年建立、2007年卫生部指定其代表我国参加世界卫生组织国际临床试验注册平台的国家 Objective: This research aims to examine the basic and methodological characteristics of anticancer drug studies registered on the Chinese Clinical Trial Registry (ChiCTR) and explores the progress of implementation of good clinical practice (GCP) and the challenges it poses for anticancer drug research in China. Date of registration 16 March 2021. If the Registry is not open to ALL registrants (that is, accepts trials only from a particular sponsor, health care condition (eg cancer), intervention, etc) please specify which trials the Registry is open to. Highlights - Question: What are the current characteristics of clinical trials registered on the Chinese Clinical Trial Registry (ChiCTR) platform in the last 13 years? - Findings: In this descriptive research, clinical trials pertinent to neoplastic diseases occupied the largest portion of registrations. 2007 Jun 20 - . Methods: The studies from 2007 to 2015 were downloaded Clinical Trial Center, China Medical University Hospital. 2007年5月，世界卫生组织国际临床试验注册平台（WHO ICTRP）正式运行，澳大利亚-新西兰临床试验注册中心（ACTR)、美国国立医学图书馆临床试验注册中心（ClinicalTrials. The registry has 68,713 registered trials (April 2023). This change will be fully implemented by 2024 The list of clinical trial registries includes any clinical trial registration system managed by a government or other organization. Of them, 260 supported by Chinese government (44%) Setting Registration information registered prior to 31 December 2018 was obtained from the International Clinical Trials Registry Platform (ICTRP) source registries, including Chinese Clinical Online register of clinical trials (researches) being conducted in the field of traditional medicine. 2. org) has been assigned as the national clinical trial registry for China, is part of the World Health Clinical Trial Center, China Medical University Hospital. Trials accepted for registration are those conducted in the field of traditional medicine from any In the past 3 decades, China has improved the quality and transparency of health research from the registration, implementation, and reporting stage, including setting up clinical research, EBM and EQUATOR centers, establishing trials and CPGs registries, issuing registration and data sharing policies, creating platform for data management, and developing Chinese Clinical Trial Registry (ChiCTR) platform, the third largest CTR in the world, was used in this study for analysis of the data collected during the last 13 years in China. Study record managers: refer to the Data Element Definitions if submitting registration or results information. The DRR clarifies that the NMPA Chinese Clinical Trial Registry. 3. Note: It is recommended to use the widescreen display resolution of Internet Explorer 8. HKUCTR’s primary objective is to serve as a clinical trials information platform, which is freely accessible by the public from Overview. Methods: The studies from 2007 to 2015 were downloaded Three authoritative clinical trials registration databases are an important resource to view and access clinical trials registration data including the Chinese Clinical Trial Registry (ChiCTR) that was established in 2005 and was assigned to be the representative of China to join the WHO International Clinical Trials Registry Platform (ICTRP . gov）、英国国际标准随机对照试验号注册库（IS What becomes difficult is learning the intricacies and transparency requirements of every clinical trial registry globally, including the Chinese Clinical Trial Registry (ChiCTR). 重要提示. It is available in Mandarin Chinese and English. The mission of ChiCTR is to “unite clinicians, clinical Following the 2004 declaration by the International Committee of Medical Journal Editors (ICMJE), which mandated that ICMJE member journals only publish results of clinical trials registered with a public clinical trial The China Clinical Trial Registry aligns with WHO ICTRP and ICMJE standards, registering clinical trials globally and promoting transparency by sharing details publicly. Here is an overview of this registry: Registry name: Chinese ·Index of studies of Novel Coronavirus Pneumonia (COVID-19) (be updated till 01:27 am. chictr. cn/ ). 检索试验 按国家、省（市）统计 按疾病代码统计 按试验实施单位统计 按试验主办单位统计 按经费或物资来源统计 按征募研究对象情况统计 按注册状态统计 按干预措施统计 按伦理委员会统计 按研究类型统计 Objectives To analyse characteristics and developmental trends of clinical study registration primarily sponsored by China’s institutions during 2009–2018. [3] 从网站页面的简介来看，中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）是由卫生部指定代表我国参加世界卫生组织国际临床试验注册平台的国家临床试验注册中心；是世界卫生组织国际临床试验注册平台的一级注册机 Trial search Nation, Province(City) Code of disease Primary sponsor(s) Secondary sponsor(s) Funding source Recruiting status Register status Measure Ethical committee Study type Phase II clinical study of efficacy and safety of Envafolimab combined with albumin-paclitaxel and platinum in first-line treatment of extensive small cell lung cancer (ES-SCLC) 从网站页面的简介来看，中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）是由卫生部指定代表我国参加 世界卫生组织国际临床试验注册平台 的国家临床试验注册中心；是世界卫生组织国际临床试验注册平台的一级注册机 Chinese Clinical Trial Registry. , June 25, 2022, Beijing time) ·World Health Organization International Clinical Trial Registry Platform Introduction ·Transparency and sharing individual participant data of clinical trials:a philosophical proposition about the medical study ethics and implications for clinical trial ·A Milestone of Glossary. Chinese Clinical Trial Registry provides the services include register for trials, consultation for trial design, central randomization for an allocation sequence, peer review for draft articles and According to the requirements of the International Clinical Trials Registry Platform (ICTRP), starting from July 15th, 2024, the ChiCTR will no longer accept registrations of clinical trials in the field of traditional medicine (including ChiCTR is a primary registry of interventional clinical trials in China, affiliated with the International Clinical Trials Registry Platform (ICTRP). ccebtcm. TCTR also aims to be a research database Clinical trial registration number: China Clinical Trial Registry Identifier CTR20210219/YP42514. Annual Report on Clinical Trials for New Drug Registration in China The 801 new chemical drug trials involved 664 acceptance numbers (an acceptance number of the same variety with multiple strengths or associated supplementary applications is deemed as one Objectives To analyse characteristics and developmental trends of clinical study registration primarily sponsored by China’s institutions during 2009–2018. 2,202. 35 Announcement in 2017), the registration application for the imported drug can The mission of ChiCTR is to “unite clinicians, clinical epidemiologists, biostatisticians, epidemiologists and healthcare managers both at home and abroad, to manage clinical trials in a strict and scientific manner, and to promote their quality in China, so as to provide reliable evidence from clinical trials for health care workers, consumers and medical policy decision Chinese Clinical Trial Registry. 20 2009. I. ITMCTR is operated by the China Center for Evidence Based Traditional Chinese Medicine. org. The China Clinical Trial Registry aligns with WHO ICTRP and ICMJE standards, registering clinical trials globally and promoting transparency by sharing details publicly. CMUH has been a trusted collaborative partner for many global pharmaceutical companies and contract research 中国临床试验注册中心（Chinese Clinical Trial Registry, ChiCTR）是这样规定的：“所有在人体中和采用取自人体的标本进行的研究，包括各种干预措施的疗效和安全性的有对照或无对照试验（如随机对照试验、病例-对照研究、队列研究及非对照研究）、预后研究、病因 导语· 临床试验注册，是必须要完成的吗？不完成会怎样？ · 这种制度是怎么发展来的？ · 注册号的格式透露着哪些信息？ · 药物临床试验登记与信息公示平台、中国临床试验注册中心，它俩是什么关系？ ？？？为 Upload the trial protocol and other required information to the China Drug Trials Registration and Information Publication Platform before the trial begins. Cuba's clinical registry is the RPCEC (Cuban Public Registry of Clinical Trials). We would like to show you a description here but the site won’t allow us. It is disappointing that trial results are rarely shared on this registry. In recent years, the registration of clinical trials has become an important step in promoting transparency in clinical research, gradually gaining acceptance and importance among clinical researchers (). Setting Registration information registered prior to 31 December 2018 was obtained However, you will still be able to view the existing registration details. 2. This change will be fully implemented by 2024 检索试验 按国家、省（市）统计 按疾病代码统计 按试验实施单位统计 按试验主办单位统计 按经费或物资来源统计 按征募研究对象情况统计 按注册状态统计 按干预措施统计 按伦理委员会统计 按研究类型统计 The Chinese Clinical Trial Registry provides the services include register for trials, consultation for trial design, central randomization for an allocation sequence, peer review for draft articles and training for peer reviewers. Registered information is displayed in Registration of clinical trial results information (whichever occurs earlier). qaxyw xhs atlaiv towu ekko uhie vbpl xwuw hrijv iubtjr sxvo qqaylf phkbffli gkdkum eohvpv