Table 1.
Randomized controlled trials | Real-world studies | ||
---|---|---|---|
Type of study | Experimental/interventional | Observational/non-interventional | Interventional/pragmatic |
Design | Prospective | Retrospective/prospective | Prospective |
Primary focus | Efficacy, safety, quality, cost-effectiveness | Efficacy, safety, quality, cost-effectiveness, natural history, compliance and adherence, service models, patient preferences, comparative | |
Patient population | Narrow, restricted, motivated | Diverse, large, and unrestricted | |
Monitoring | Intense (ICH-GCP compliant) | Not required (?) | Reflects usual care |
Comparators | Gold standard/placebo | None/standard clinical practice/multiple iterations | Standard practice/placebo/multiple iterations |
Outcomes | Clear sequence | Wide range | |
Data collection confounders | Standardized, controlled | Routine, recruitment bias (?), recall/interviewer bias | |
Randomization | Yes | No | Yes |
Blinding | Yes | No | Sometimes (participants or outcome assessment) |
Follow-up | Generally short | Reflects usual care | Long |
ICH-GCP International Conference on Harmonisation of Good Clinical Practice