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 @ 5:36 PM
Ignite Modification Date:
2025-12-25 @ 3:07 PM
NCT ID:
NCT01091168
Group ID:
EG001
Title:
Alkylating Agent
Description:
Patients randomised in the control arm (arm B) received an alkylating agent used as a single agent which was available in the investigational center and was approved for the treatment of cancer in the country.
Alkylating agent of physician choice registered in cancer: cyclophosphamide or melphalan or mitomycin C or thiotepa or cisplatin or carboplatin
Deaths Number Affected:
274
Deaths Number At Risk:
None
Serious Number Affected:
66
Serious Number At Risk:
290
Other Number Affected:
262
Other Number At Risk:
290
Study:
NCT01091168
Results Section:
NCT01091168
Adverse Events Module:
NCT01091168