Loading
Trials and hospital records describe the same things in different languages. Publish the translation so trial patients can be followed for life in routine data and trial results compared with routine care.
Clinical trial data follow CDISC standards; routine data follow mCODE or OMOP. Formal, maintained mappings (CDISC to mCODE, CDISC to OMOP) would allow trial participants to be followed via registries after the trial ends, trial cohorts to be compared with matched real-world cohorts, and completed trial datasets to be pooled with routine data. CDISC and HL7 have a joint project; the proposal funds it to completion and requires sponsors to deliver the mapped dataset alongside submissions.
Shares ClinicalTrials.gov, Data silos.
Shares ClinicalTrials.gov, Trial design, endpoints and cost.
Every source this page cites, grouped by who published it. Grouping is read from the web address, not assigned by hand.
A source that has moved or gone is reported by the weekly link check. /audit/