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 @ 4:17 AM
Ignite Modification Date:
2025-12-26 @ 3:18 AM
NCT ID:
NCT01489020
Group ID:
EG002
Title:
Group C Active
Description:
8 administrations, 2 administrations in the same day. 1 week interval between 2 doses, during 3 weeks.
1. Week 1: vial 2 - 2 administrations of 0.1 ml with 30 minute interval
2. Week 2: vial 2 - 0.2 ml and 0.3 ml with 30 minute interval
3. Week 3: vial 3 - 2 doses of 0.1 ml with 30 minute interval
4. Week 4: vial 3 - 0.2 ml and 0.3 ml with 30 minute interval
subcutaneous immunotherapy with DPT extract: Increasing doses of subcutaneous immunotherapy in three different scales up to the maximum dose of 500 TSU (Treatment Standardized Units) or placebo
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
12
Other Number Affected:
8
Other Number At Risk:
12
Study:
NCT01489020
Results Section:
NCT01489020
Adverse Events Module:
NCT01489020