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 @ 7:02 PM
Ignite Modification Date:
2025-12-25 @ 4:36 PM
NCT ID:
NCT00270257
Group ID:
EG000
Title:
Long Term Medication Assisted Treatment (LT-MAT)
Description:
Participants will receive BUP/NX under the tongue daily for a maximum of three weeks(until dose stabilization) and then three times a week for 52 weeks in addition to weekly drug and risk reduction counseling for 12 weeks, and then every 4 weeks through Week 52
Buprenorphine/Naloxone: Oral tablet
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
623
Other Number Affected:
0
Other Number At Risk:
623
Study:
NCT00270257
Results Section:
NCT00270257
Adverse Events Module:
NCT00270257