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:
NCT00203502
Group ID:
EG000
Title:
Intervention: Drug:Docetaxel + Cyclophosphamide + Avastin
Description:
Docetaxel 75mg/m2 + Cyclophosphamide 500 mg/m2
\+ Avastin 15 mg/kg
Q 3 weeks X 4 cycles
Bevacizumab/Avastin: IV 15mg/kg 21 days
Cyclophosphamide: 500mg per meter squared, IV every 21 days
Doxorubicin: 60 mg per meter squared, IV every 21 days
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
39
Serious Number At Risk:
39
Other Number Affected:
19
Other Number At Risk:
39
Study:
NCT00203502
Results Section:
NCT00203502
Adverse Events Module:
NCT00203502