So sánh phương pháp

	Thử nghiệm lâm sàng Giai đoạn II được khớp cặp	Ghép cặp điểm xu hướng
Lĩnh vực	Dịch tễ học	Thống kê nghiên cứu
Họ	Process / pipeline	Process / pipeline
Năm ra đời	1960s–1980s (formalized with Simon optimal designs, 1989)	1983
Người khởi xướng	Gehan (1961) for Phase II designs; matching frameworks adapted from case-control methodology	Paul Rosenbaum and Donald Rubin
Loại	Controlled clinical trial design	Method
Công trình gốc	Gehan, E. A. (1961). The determination of the number of patients required in a preliminary and a follow-up trial of a new chemotherapeutic agent. Journal of Chronic Diseases, 13(4), 346–353.	Rosenbaum, P. R., & Rubin, D. B. (1983). The central role of the propensity score in observational studies for causal effects. Biometrika, 70(1), 41–55.
Tên gọi khác	matched Phase II trial, historically matched Phase II study, propensity-matched Phase II trial, externally controlled Phase II trial	PSM, propensity score weighting, covariate balance
Liên quan	5	3
Tóm tắt	A matched Phase II clinical trial is a single-arm or small-controlled early-efficacy study in which treated patients are paired with matched controls — drawn from historical databases, registries, or concurrent external cohorts — on key prognostic variables such as age, disease stage, and performance status. This design allows preliminary efficacy assessment without a concurrent randomized arm, trading randomization for feasibility while partially controlling for confounding through the matching process.	Propensity score matching (PSM) is a method for reducing confounding bias in observational studies by balancing baseline characteristics between treatment groups, simulating randomization. Developed by Rosenbaum and Rubin (1983), it estimates the probability of receiving treatment given observed covariates, then matches or weights treated and control individuals with similar treatment probabilities. Widely used in medicine, epidemiology, and policy evaluation when randomized trials are infeasible or unethical, enabling estimation of treatment effects while controlling for selection bias.