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 @ 9:24 PM
Ignite Modification Date:
2025-12-25 @ 7:10 PM
NCT ID:
NCT01468532
Group ID:
EG000
Title:
Treatment (Chemotherapy, Receptor Agonist)
Description:
Patients receive pasireotide IM on day 1, docetaxel IV over 1 hour, and prednisone PO BID continuously. Courses with docetaxel repeat every 21 days and courses with pasireotide repeat every 28 days in the absence of disease progression or unacceptable toxicity.
docetaxel: Given IV
pasireotide: Given IM
prednisone: Given PO
Deaths Number Affected:
13
Deaths Number At Risk:
None
Serious Number Affected:
14
Serious Number At Risk:
18
Other Number Affected:
18
Other Number At Risk:
18
Study:
NCT01468532
Results Section:
NCT01468532
Adverse Events Module:
NCT01468532