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 @ 12:18 PM
Ignite Modification Date:
2025-12-25 @ 12:02 PM
NCT ID:
NCT01422161
Group ID:
EG000
Title:
Botulinum Toxin Commonly Known as BOTOX®
Description:
Some subjects will receive BOTOX® injections. Subject will not be informed of what injection they received.
Botulinum Toxin commonly known as BOTOX®: A total dose between 200-300 units of Botulinum toxin will be administered across 12 muscles of the affected hand.
The control group will receive a placebo injection. There will be 1 treatment cycle during the 9 week study.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
10
Other Number Affected:
0
Other Number At Risk:
10
Study:
NCT01422161
Results Section:
NCT01422161
Adverse Events Module:
NCT01422161