Comparar métodos

	Estudo de Caso-Controle	Ensaio Clínico Randomizado (ECR)
Área	Epidemiologia	Epidemiologia
Família	Process / pipeline	Process / pipeline
Ano de origem	1950s (formal methodology); precursors in the 1920s	1948 (first rigorously conducted RCT — MRC streptomycin trial)
Autor original	Janet Lane-Claypon (early precursors, 1926); formalized by Brian MacMahon and Jerome Cornfield in the 1950s–1960s	Austin Bradford Hill; MRC Streptomycin Trial team
Tipo	Observational analytic study design	Interventional experimental study
Fonte seminal	Schlesselman, J.J. (1982). Case-Control Studies: Design, Conduct, Analysis. Oxford University Press. ISBN: 978-0195027860	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
Outros nomes	case-referent study, case-control design, retrospective case-control, case-control analysis	RCT, randomized controlled trial, randomised controlled trial, clinical randomized trial
Relacionados	6	6
Resumo	A case-control study is a retrospective observational design in which individuals who have developed a disease or outcome of interest (cases) are compared with individuals who have not (controls) to determine whether prior exposure to a putative risk factor differs between the two groups. The primary measure of association is the odds ratio, which approximates the relative risk when the outcome is rare. Case-control studies are especially efficient for investigating rare diseases and generating etiological hypotheses.	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.