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 @ 12:13 AM
Ignite Modification Date:
2025-12-25 @ 10:14 PM
NCT ID:
NCT01800058
Group ID:
EG000
Title:
Circulating Prostatic Tumor Cells in the Peripheral Blood
Description:
Patients that satisfy inclusion criteria, and after signing informed consent, will extract 1 blood sample (7.5 mL):
1. prior to any treatment;
2. following AD and prior to RT; and
3. following the end of RT (1-3 months afterwards).
The quantification of CTC in blood samples will be done with the CellSearch® system.
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
65
Other Number Affected:
15
Other Number At Risk:
65
Study:
NCT01800058
Results Section:
NCT01800058
Adverse Events Module:
NCT01800058