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:
2025-12-25 @ 3:45 AM
Ignite Modification Date:
2025-12-26 @ 2:32 AM
NCT ID:
NCT01987102
Group ID:
EG000
Title:
Cohort 1
Description:
1 MAP cycle (incl. 2 HDMTX courses with SOC rescue 15mg/m2)
1 MAP cycle (incl. 2 HDMTX courses with MOD rescue 15mg/m2)
SOC was administered as rescue in the 2 first HDMTX courses and MOD in the 2 following courses.
Treatment according to the MAP schedule applied. SOC or MOD commenced 24 h after administration of HDMTX and then every 6 h until the serum-MTX levels were ≤ 0.1 µmol/L, in accordance with COG management recommendations.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
8
Other Number Affected:
4
Other Number At Risk:
8
Study:
NCT01987102
Results Section:
NCT01987102
Adverse Events Module:
NCT01987102