Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 10:54 PM
Ignite Modification Date:
2025-12-25 @ 8:23 PM
NCT ID:
NCT00534469
Group ID:
EG000
Title:
HD ARA-C With or Without Idarubicin
Description:
This study was designed as a single-arm study.
Strata were:
HD ARA-C w/ Idarubicin, CR\<6 months N = 24 patients. HD ARA-C w/ Idarubicin, CR\>6 months N=1. HD ARA-C consolidation, CR\<6 months N=5. HD ARA-C consolidation, CR\>6 months N= 0.
aldesleukin
filgrastim
busulfan
cytarabine
etoposide
idarubicin
autologous hematopoietic stem cell transplantation
bone marrow transplantation
peripheral blood stem cell transplantation
total-body irradiation
Deaths Number Affected:
37
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
60
Other Number Affected:
47
Other Number At Risk:
60
Study:
NCT00534469
Results Section:
NCT00534469
Adverse Events Module:
NCT00534469