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 @ 4:12 AM
Ignite Modification Date:
2025-12-26 @ 3:11 AM
NCT ID:
NCT00658320
Group ID:
EG001
Title:
Mycophenolate Mofetil (MMF) + Standard Dose of Cyclosporine
Description:
Patients were treated with 1 gram twice a day (2 grams/day) of Mycophenolate mofetil (MMF) and standard dose of cyclosporine for 12 months post renal transplant. Patients were treated with antibody induction therapy using 20 mg basiliximab two hours prior to transplant and 20 mg basiliximab 4 days post transplant or according to local practice. Corticosteroids were administered according to local practice. Patients were treated for 12 months in the core study and 12 months in the extension study.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
37
Serious Number At Risk:
61
Other Number Affected:
61
Other Number At Risk:
61
Study:
NCT00658320
Results Section:
NCT00658320
Adverse Events Module:
NCT00658320