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 @ 4:04 AM
Ignite Modification Date:
2025-12-26 @ 2:59 AM
NCT ID:
NCT00992602
Group ID:
EG000
Title:
Treatment (Liposomal Cytarabine, High-dose Methotrexate)
Description:
Induction phase: All patients receive 3 doses of High-Dose Methotrexate (HD-MTX) every 2 weeks given intravenously and 3 doses of Intrathecal (IT) Liposomal Cytarabine (Depocyt) every 2 weeks over 6 weeks.
Consolidation phase:
2 additional doses of HD-MTX every 2 weeks and IT-Depocyt every 2 weeks for 4 more weeks.
Maintenance phase:
Monthly doses of HD-MTX (up to 6 doses) and IT-Depocyt (up to 5 doses)
Patients must stop participation anytime MRI shows progressive disease or positive CSF cytology.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
3
Other Number Affected:
2
Other Number At Risk:
3
Study:
NCT00992602
Results Section:
NCT00992602
Adverse Events Module:
NCT00992602