ScholarGate
Assistant

Comparer des méthodes

Examinez les méthodes sélectionnées côte à côte ; les lignes qui diffèrent sont mises en évidence.

Essai clinique de phase III méta-analytique×Méta-analyse de données individuelles de patients×
DomaineÉpidémiologieSynthèse des données probantes
FamilleProcess / pipelineProcess / pipeline
Année d'origine1976 (meta-analysis); systematic application to Phase III RCTs from 1990s onward1990s
Auteur d'origineGlass, G. V. (meta-analysis formalized); applied to Phase III trials via Cochrane Collaboration (Chalmers, Altman, Higgins)Cochrane Collaboration, Pioneered by Stewart & Clarke
TypeSystematic quantitative evidence synthesisMethod
Source fondatriceWhitehead, A. (2002). Meta-Analysis of Controlled Clinical Trials. Wiley. ISBN: 978-0471983705Stewart, L. A., Clarke, M. J., & Cochrane IPD Meta-analysis Methods Group. (2015). Practical methodology of meta-analyses (including IPD) of randomised trials reporting time to event data. Cochrane Database of Systematic Reviews, 2015(10), MR000027. link ↗
AliasPhase III meta-analysis, pooled Phase III analysis, systematic review of Phase III RCTs, confirmatory meta-analysisIPD Meta-Analysis, Participant-Level Data Synthesis, One-Stage Meta-Analysis
Apparentées31
RésuméA meta-analytic Phase III clinical trial is a systematic, quantitative synthesis of multiple Phase III randomized controlled trials (RCTs) examining the same intervention. By pooling confirmatory trial data under a pre-registered protocol, the approach yields more precise effect estimates, resolves conflicting findings across trials, and supports regulatory or clinical guideline decisions with the highest level of evidence available in the evidence hierarchy.Individual patient data meta-analysis (IPD-MA) is a systematic synthesis method where researchers obtain and analyze raw data at the patient level from multiple randomized controlled trials, rather than relying on published summary statistics (aggregate data). Pioneered by the Cochrane Collaboration and formalized by Stewart, Clarke, and Riley, IPD-MA is considered the gold standard for evidence synthesis because it enables consistent outcome definition across trials, robust subgroup analysis, and detection of treatment-covariate interactions. Though time-intensive and resource-demanding, IPD-MA provides the most reliable estimates of intervention effects and is preferred for critical clinical decisions, particularly for identifying which patients benefit most from treatment.
ScholarGateJeu de données
  1. v1
  2. 2 Sources
  3. PUBLISHED
  1. v1
  2. 3 Sources
  3. PUBLISHED

Aller à la recherche Télécharger les diapositives

ScholarGateComparer des méthodes: Meta-analytic Phase III Clinical Trial · Individual Patient Data Meta-Analysis. Consulté le 2026-06-20 sur https://scholargate.app/fr/compare