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 @ 12:30 AM
Ignite Modification Date:
2025-12-25 @ 10:37 PM
NCT ID:
NCT00243867
Group ID:
EG001
Title:
Paclitaxel and Carboplatin
Description:
Paclitaxel 225 mg/m² intravenously followed immediately by carboplatin AUC = 6 mg\*min/mL. Paclitaxel and carboplatin were given up to 6 treatment cycles.
Carboplatin: Administered by intravenous infusion over 30 minutes. Dosing was based on the Calvert formula: carboplatin dose (mg) = (Target AUC) x (glomerular filtration rate \[GFR\] + 25).
Paclitaxel: Administered by intravenous infusion over 3 hour infusion
Deaths Number Affected:
196
Deaths Number At Risk:
None
Serious Number Affected:
91
Serious Number At Risk:
251
Other Number Affected:
239
Other Number At Risk:
251
Study:
NCT00243867
Results Section:
NCT00243867
Adverse Events Module:
NCT00243867