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 @ 4:25 AM
Ignite Modification Date:
2025-12-26 @ 3:29 AM
NCT ID:
NCT02709720
Group ID:
EG000
Title:
Experimental Group
Description:
2 cycles of metronomic Vinorelbine 50 mg + cisplatin, followed by 2 cycles of Vinorelbine 30 mg + cisplatin concomitant with radiotherapy
Vinorelbine: Cycle 1 and 2 50 mg/day, (Monday, Wednesday and Friday)
Cisplatin: Cycle 1 and 2 day 1, 80 mg/m2
Vinorelbine: Cycle 3 and 4 30 mg/day, (Monday, Wednesday and Friday)
Cisplatin: Cycle 3 and 4 day 1, 80 mg/m2
Radiotherapy: concomitant therapy during cycles 3 and 4. Total dose: 66Gy
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
65
Other Number Affected:
64
Other Number At Risk:
65
Study:
NCT02709720
Results Section:
NCT02709720
Adverse Events Module:
NCT02709720