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 @ 2:50 AM
Ignite Modification Date:
2025-12-26 @ 1:31 AM
NCT ID:
NCT03098433
Group ID:
EG000
Title:
Three Treatments in Random Order
Description:
Each participant will receive a single dose of lithyronine, a single dose of levothyroxine, and a single dose of placebo, in a random order.
Information on the order of treatments was not collected.
Participants will attend three study visits. At the first study visit one of the three treatments will be randomly selected and administered.
At the second study visit one of the remaining two treatments will be randomly selected and administered.
At the third study visit the final treatment will be administered.
The order of administration will not be tracked.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
12
Other Number Affected:
0
Other Number At Risk:
12
Study:
NCT03098433
Results Section:
NCT03098433
Adverse Events Module:
NCT03098433