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| Thử nghiệm lâm sàng ngẫu nhiên (RCT)× | Giai đoạn III Thử nghiệm lâm sàng× | |
|---|---|---|
| Lĩnh vực | Dịch tễ học | Dịch tễ học |
| Họ | Process / pipeline | Process / pipeline |
| Năm ra đời≠ | 1948 (first rigorously conducted RCT — MRC streptomycin trial) | 1962 (Kefauver-Harris Amendment formalised phased drug development) |
| Người khởi xướng≠ | Austin Bradford Hill; MRC Streptomycin Trial team | FDA regulatory framework / ICH guidelines |
| Loại≠ | Interventional experimental study | Confirmatory randomised controlled trial |
| Công trình gốc | 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 | 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 |
| Tên gọi khác | RCT, randomized controlled trial, randomised controlled trial, clinical randomized trial | Phase 3 trial, confirmatory trial, pivotal trial, Phase III RCT |
| Liên quan | 6 | 6 |
| Tóm tắt≠ | A randomized clinical trial (RCT) is an experimental study design in which participants are randomly assigned to an intervention group or a control group, then followed prospectively to compare outcomes. Random allocation is the defining feature: it distributes known and unknown confounders across groups by chance, making the RCT the strongest individual study design for establishing causal efficacy of a treatment or intervention under controlled conditions. | A Phase III clinical trial is a large-scale, confirmatory randomised controlled trial designed to establish the efficacy and safety of an intervention in the target patient population before regulatory submission. It builds on the signal identified in Phase II, tests the intervention at its proposed dose under controlled conditions, and provides the primary evidence base for marketing authorisation or guideline adoption. |
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