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 @ 5:30 PM
Ignite Modification Date:
2025-12-25 @ 3:04 PM
NCT ID:
NCT00099268
Group ID:
EG000
Title:
Carbidopa/Levodopa/Entacapone
Description:
Patients received Carbidopa/levodopa/entacapone tablets. The study was designed as a flexible dose trial (200-1000 mg/day levodopa). The target dose was 400 mg/day levodopa administered orally as 4 equal doses 4 times a day with 3.5-hour dosing intervals for a treatment period of 134 to 208 weeks.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
91
Serious Number At Risk:
373
Other Number Affected:
310
Other Number At Risk:
373
Study:
NCT00099268
Results Section:
NCT00099268
Adverse Events Module:
NCT00099268