Порівняння методів
Переглядайте обрані методи поруч; рядки з відмінностями підсвічено.
| Прагматичне рандомізоване контрольоване дослідження× | Багатоцентрове рандомізоване контрольоване дослідження× | |
|---|---|---|
| Галузь | Епідеміологія | Епідеміологія |
| Родина | Process / pipeline | Process / pipeline |
| Рік появи≠ | 1967 | 1970s–1980s (widespread adoption for large-scale efficacy trials) |
| Автор методу≠ | Daniel Schwartz & Joseph Lellouch | Evolved from single-center RCT methodology; consolidated through landmark trials such as the MRC streptomycin trial (1948) and large cardiovascular mega-trials of the 1970s–1980s |
| Тип≠ | Interventional study design | Interventional experimental design |
| Основоположне джерело≠ | Schwartz, D., & Lellouch, J. (1967). Explanatory and pragmatic attitudes in therapeutical trials. Journal of Chronic Diseases, 20(8), 637–648. DOI ↗ | Friedman, L. M., Furberg, C. D., DeMets, D. L., Reboussin, D. M., & Granger, C. B. (2015). Fundamentals of Clinical Trials (5th ed.). Springer. ISBN: 978-3319185385 |
| Інші назви | pragmatic RCT, effectiveness trial, real-world RCT, practical clinical trial | multi-site RCT, multicenter RCT, multinational randomized trial, multicenter controlled trial |
| Пов'язані | 6 | 6 |
| Підсумок≠ | A pragmatic randomized clinical trial (pragmatic RCT) is an interventional study that tests whether a treatment works under routine clinical conditions, as opposed to the tightly controlled setting of an explanatory trial. It prioritizes broad eligibility, flexible delivery, and patient-relevant outcomes to answer the question 'Does this treatment work in everyday practice?' rather than 'Can this treatment work under ideal circumstances?' The distinction between pragmatic and explanatory trials was formally articulated by Schwartz and Lellouch in 1967 and operationalized by the PRECIS tool in 2009. | A multicenter randomized clinical trial (RCT) is an experimental study in which eligible participants are randomly assigned to intervention or control arms simultaneously across two or more clinical sites. By combining the rigor of randomization with enrollment from geographically or institutionally diverse centers, this design produces large samples and externally valid effect estimates that single-center trials rarely achieve. It is the regulatory gold standard for confirmatory efficacy and safety evaluation of new treatments. |
| ScholarGateНабір даних ↗ |
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