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 @ 4:07 AM
Ignite Modification Date:
2025-12-26 @ 3:04 AM
NCT ID:
NCT01950520
Group ID:
EG014
Title:
Cohort 2 : Topiramate
Description:
Interventions, in random order, will be administered during one of the six one-day stays
Caffeine: Caffeine 200mg, oral, by mouth (Cohort 2 only)
Qsymia: Qsymia (topiramate 92mg CR, phentermine 15mg PO), oral, by mouth (Cohort 2 only)
Topiramate: Topiramate 200mg, oral, by mouth (Cohort 2 only)
Phentermine: Phentermine 37.5mg, oral, by mouth (Cohort 2 only)
Naltrexone: Naltrexone 100mg, oral, by mouth (Cohort 2 only)
Placebo Cohort 2: Placebo, oral, by mouth (Cohort 2 only)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
18
Other Number Affected:
5
Other Number At Risk:
18
Study:
NCT01950520
Results Section:
NCT01950520
Adverse Events Module:
NCT01950520