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The ICTRP is a global initiative that aims to make information about all clinical trials involving humans publicly available. It also aims to: improve the comprehensiveness, completeness and accuracy of registered clinical trial data; communicate and raise awareness of the need to register clinical trials; ensure the accessibility of registered ...
The ICTRP is a country-led initiative. Clinical trial registration happens when countries seek to improve the transparency of clinical trial research involving nationals of that country, and to be more accountable to the individuals who consent to participate in clinical research, and to better oversee and monitor that research.
This guidance updates and adapts the previous work of the World Health Organization (WHO) on research capacity for the context of well-designed and well-implemented clinical trials as framed in resolution WHA75.8 (2022). It aims to enhance clinical research efficiency, minimize research waste and provide guidance on sustained clinical trials that are always functional and active for endemic ...
For the purposes of registration, a clinical trial is any research study that prospectively assigns human participants or groups of humans to one or more health-related interventions to evaluate the effects on health outcomes. Clinical trials may also be referred to as interventional trials.
A randomized clinical trial performed in the Netherlands reported that imatinib might confer clinical benefit in hospitalized Covid-19 patients, in the absence of safety issues. Infliximab produced by Johnson and Johnson, is used to treat diseases of the immune system.
In May 2022, the Seventy-fifth World Health Assembly adopted a resolution (WHA75.8) on “Strengthening clinical trials to provide high-quality evidence on health interventions and to improve research quality and coordination”. The WHO secretariat has developed this webpage in order to provide a single point of access for information and ...
-- In 2009, trial registration was added as a requirement of ethical guidelines for medical research in Japan. However, both countries reported a decrease between 2021 and 2022 (select China and Japan respectively in chart C, and view chart A and chart B).
number of trial participants (chart H) Chart A shows the total number of trials, regardless of the number of trial sites involved. A multicountry trial is counted once for each participating region in chart C but once for each participating country in chart E. The default for other charts is one trial counted once regardless of the number of sites.
The ICTRP Search Portal aims to provide a single point of access to information about ongoing and completed clinical trials. 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.
The World Health Organization (WHO) today released guidance to improve the design, conduct and oversight of clinical trials in countries of all income levels. This guidance aims to support stronger country-led research and development (R&D) ecosystems to advance health science so that new, safe and effective health interventions can be made more accessible and affordable globally for people ...