Importance of swift event adjudication of endpoints for adequate reporting to data and safety monitoring boards in clinical trials-lessons from CULPRIT-SHOCK
Trials
.
2021 Mar 8;22(1):197.
doi: 10.1186/s13063-021-05129-4.
Authors
Peter Clemmensen
1
,
Benedikt Schrage
2
,
Uwe Zeymer
3
,
Holger Thiele
4
,
Karl Wegscheider
5
Affiliations
1
University Heart and Vascular Center Hamburg, Department of Cardiology, Hamburg, Germany.
2
University Heart and Vascular Center Hamburg, Department of Cardiology, Hamburg, Germany. b.schrage@uke.de.
3
Klinikum Ludwigshafen, Ludwigshafen am Rhein, Germany.
4
Heart Center Leipzig at University of Leipzig and Leipzig Heart Institute, Leipzig, Germany.
5
University Hospital Hamburg Eppendorf, Hamburg, Germany.
PMID:
33685472
PMCID:
PMC7941876
DOI:
10.1186/s13063-021-05129-4
No abstract available
Publication types
Letter
Comment
MeSH terms
Clinical Trials Data Monitoring Committees*
Humans
Magnetic Resonance Imaging
Shock*