The list of clinical trial registries includes any clinical trial registration system managed by a government or other organization.
The World Health Organization's International Clinical Trials Registry Platform (ICTRP) acts as a voluntary coordinating body for many international registries, including many of those listed below.
The Pan-African clinical trials registry (PACTR) is available at pactr.org. It is funded by the European and Developing Countries Clinical Trials Partnership (EDCTP) and operates out of the South African Cochrane Centre (Cochrane Collaboration) based at the South African Medical Research Council. PACTR contributes data to the WHO's ICTRP.
Australia and New Zealand share the ANZCTR registry located at: anzctr.org.au. Registering trials with the ANZCTR is voluntary. It is publicly owned and managed by a non-profit organization and is funded by an enabling grant from Australia's National Health and Medical Research Council (NHMRC). [1]
Brazil has a registry (Registro Brasileiro de Ensaios Clínicos, ReBEC): ensaiosclinicos.gov.br. ReBEC is a project of the Brazilian Ministry of Health, the Panamerican Health Organization (PAHO) and the Oswaldo Cruz Foundation (FIOCRUZ).
The Canadian Institutes of Health Research (CIHR) participates with the ISRCTN.
China's clinical trial registry is called ChiCTR: chictr.org.cn. It is available in Mandarin Chinese and English. It was established in October 2005. It participates in the WHO's ICTRP. [2]
Cuba's clinical registry is the RPCEC (Cuban Public Registry of Clinical Trials). [3]
EudraCT is a database of all clinical trials conducted in the European Union since 1 May 2004. Initially a non-public database, it was launched for the public as EU Clinical Trials Register in March 2011.
Germany's clinical trials registry, the DRKS, is available at drks.de. The DRKS is an open access, free of charge online register for clinical trials and is available both in English and German. DRKS is part of the WHO's ICTRP. The DRKS works with two partner registries in Germany, DeReG (German Registry for Somatic Gene-Transfer Trials) and Clinical Trial Registry of the University Medical Center Freiburg. [4]
India's clinical trials registry is Clinical Trials Registry – India. CTRI is in English and it participates in the WHO's ICTRP. [2]
Iran's registry, the IRCT, is available at irct.ir. It is run and funded by the Iranian Ministry of Health and Medical Education. [5]
Japan has three registries that work as a network called the Japan Primary Registries Network (JPRN). Its search portal is hosted by the Japanese National Institute of Public Health. [6] While the search portal is only available in Japanese, the three registries' sites are also available in English:
The Netherlands registry participates with WHO and its website is trialregister.nl. Clinical trial data are available in English.
South Africa’s Department of Health announced in November 2005, that clinical trials conducted in the country must be submitted to the South African National Clinical Trials Register located at: sanctr.gov. Clinical trial guidelines for South Africa are available at the Department of Health's official site. [7]
South Korea's registry is Clinical Research Information Service (CRiS) and available at https://web.archive.org/web/20101121001837/http://ncrc.cdc.go.kr/cris/index.jsp. It is managed by the Korea Centers for Disease Control and Prevention and funded by South Korea's Ministry of Health and Welfare. [8]
The Sri Lanka Clinical Trials Registry (SLCTR) is available at slctr.lk. It is funded by the Sri Lanka Medical Association and managed by the Sri Lanka Clinical Trials Registry Committee. [9]
The ISRCTN registry was launched in 2000. Originally ISRCTN stood for 'International Standard Randomised Controlled Trial Number'; however, the scope of the registry has widened beyond randomized controlled trials to include any study designed to assess the efficacy of health interventions in a human population. It registers both observational and interventional trials and content is curated by a team of expert editors.
This section needs to be updated. The reason given is: Add information about HHS making public more information about clinical trials (see link).(September 2016) |
Clinical trials in the US are registered on clinicaltrials.gov. Clinicaltrials.gov is the largest clinical trials registry. Clinical trials conducted in the United States are required to be registered in the registry. Its registrations represent about 75% of what is available through the WHO portal (ICTRP). Problems of concordance between ClinicalTrials.gov records and published records have been identified for many protocol and results items. [10] The registry traces back to the Health Omnibus Programs Extension Act of 1988 (HOPE or Public Law 100-607) which mandated the development of a database of AIDS Clinical Trials Information System. It would later be expanded under the Food and Drug Administration Modernization Act of 1997 (FDAMA or Public Act 105-115). The registry is run by the United States National Library of Medicine (NLM).
Clinical trial registries are also set up and managed by governmental organizations, non-governmental organizations, universities, as well as commercial and nonprofit entities. This includes pharmaceutical companies, international organizations, and health organizations. A list is available at http://www.circare.org/registries.htm.
The IFPMA Clinical Trials Portal is a major pharmaceutical industry initiative designed to increase the transparency of clinical trials by providing a convenient "one-stop-shop" for published clinical trial information. It helps to fulfill the commitment made by the research-based pharmaceutical industry in its Joint Position on the Disclosure of Clinical Trial Information via Clinical Trial Registries and Databases. It is available here.
BioMed Central (BMC) is a United Kingdom-based, for-profit scientific open access publisher that produces over 250 scientific journals. All its journals are published online only. BioMed Central describes itself as the first and largest open access science publisher. It was founded in 2000 and has been owned by Springer, now Springer Nature, since 2008.
The regulation of therapeutic goods, defined as drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as in Australia.
.lk is the Internet country code top-level domain (ccTLD) for Sri Lanka. Foreign companies who do not have a local presence can only reserve their top-level and corresponding open second-level domains. In order to register and use a name they must have a contact address in Sri Lanka.
Pharmacovigilance, also known as drug safety, is the pharmaceutical science relating to the "collection, detection, assessment, monitoring, and prevention" of adverse effects with pharmaceutical products. The etymological roots for the word "pharmacovigilance" are: pharmakon and vigilare. As such, pharmacovigilance heavily focuses on adverse drug reactions (ADR), which are defined as any response to a drug which is noxious and unintended, including lack of efficacy. Medication errors such as overdose, and misuse and abuse of a drug as well as drug exposure during pregnancy and breastfeeding, are also of interest, even without an adverse event, because they may result in an adverse drug reaction.
Medical research, also known as health research, refers to the process of using scientific methods with the aim to produce knowledge about human diseases, the prevention and treatment of illness, and the promotion of health.
Dr. Oscar Kashala Lukumuena is a Boston-based scientist, clinical researcher, university professor, and senior executive in the biopharmaceutical industry in the United States of America (USA). He is a politician in the Democratic Republic of the Congo and was a reformer candidate in the 2006 presidential election and 2011 presidential elections.
Pharmaceutical policy is a branch of health policy that deals with the development, provision and use of medications within a health care system. It embraces drugs, biologics, vaccines and natural health products.
Orphanet is an organisation and knowledge base dedicated to rare diseases as well as corresponding diagnosis, orphan drugs, clinical trials and expert networks.
The Epidemiology Data Center (EDC) is recognized as an official University Center at the University of Pittsburgh; and is part of the Department of Epidemiology at the University of Pittsburgh Graduate School of Public Health. The EDC was formed in 1980 by Katherine M. Detre, M.D., Dr.P.H., and is currently under the co-direction of Maria Mori Brooks, Ph.D., Steven H. Belle, Ph.D. and Stephen R. Wisniewski, Ph.D.
ClinicalTrials.gov is a registry of clinical trials. It is run by the United States National Library of Medicine (NLM) at the National Institutes of Health, and holds registrations from over 444,000 trials from 221 countries.
AllTrials is a project advocating that clinical research adopt the principles of open research. The project summarizes itself as "All trials registered, all results reported": that is, all clinical trials should be listed in a clinical trials registry, and their results should always be shared as open data.
Vonoprazan, sold under the brand name Voquezna among others, is a first-in-class potassium-competitive acid blocker medication. Vonoprazan is used in form of the fumarate for the treatment of gastroduodenal ulcer and reflux esophagitis, and can be combined with antibiotics for the eradication of Helicobacter pylori. It is a potassium-competitive acid blocker.
The Japan Medical Association, is the largest professional association of licensed physicians in Japan. The JMA has been a member of the World Medical Association since 1951 and participates at all levels of the WMA. National headquarters are located in Honkomagome, Bunkyō, Tokyo, Japan, supplemented by prefectural branch offices and member associations in local communities.
Preregistration is the practice of registering the hypotheses, methods, and/or analyses of a scientific study before it is conducted. Clinical trial registration is similar, although it may not require the registration of a study's analysis protocol. Finally, registered reports include the peer review and in principle acceptance of a study protocol prior to data collection.
Jiangsu Hengrui Pharmaceuticals Company Ltd., also known as Jiangsu Hengrui, is a Chinese pharmaceutical company that manufactures and distributes various types of drug packaging materials, cancer-treating antineoplastics, cardiovascular medication, painkillers, antibiotics, and related products. It is the largest listed pharmaceutical company in China.
The International Clinical Trials Registry Platform (ICTRP) is a platform for the registration of clinical trials operated by the World Health Organization.
COVIran Barekat is a COVID-19 vaccine developed in Iran by Shifa Pharmed Industrial Group, a subsidiary of the Barkat Pharmaceutical Group. It is an inactivated virus-based vaccine. Iranian authorities have authorized its emergency use. This makes it the first locally developed COVID-19 vaccine to be approved for emergency use in the Middle East.
The Sanofi–GSK COVID-19 vaccine sold under the brand name VidPrevtyn Beta, is a COVID-19 vaccine developed by Sanofi Pasteur and GSK.
FAKHRAVAC is a COVID-19 vaccine developed in Iran by the Organization of Defensive Innovation and Research, a subsidiary of Iran's Ministry of Defense. It is the third Iranian COVID-19 vaccine reaching clinical trials. It is currently in phase III. It received emergency use authorization in Iran on 9 September 2021.
COVID-19 vaccine clinical research uses clinical research to establish the characteristics of COVID-19 vaccines. These characteristics include efficacy, effectiveness, and safety. As of November 2022, 40 vaccines are authorized by at least one national regulatory authority for public use: