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 @ 3:27 AM
Ignite Modification Date:
2025-12-26 @ 2:07 AM
NCT ID:
NCT01618305
Group ID:
EG001
Title:
Arm B (Women)
Description:
Pregnant women received ZDV/3TC + RAL
Lamivudine/zidovudine: Participants received one lamivudine 150 mg/zidovudine 300 mg fixed-dose combination tablet twice a day from entry through delivery\*.
\* Participants may have received a locally supplied nucleoside reverse transcriptase inhibitor (NRTI) backbone in place of lamivudine/zidovudine with permission of the protocol team obtained prior to randomization.
Raltegravir: Participants received one 400 mg raltegravir tablet twice a day from entry through delivery.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
34
Serious Number At Risk:
206
Other Number Affected:
24
Other Number At Risk:
206
Study:
NCT01618305
Results Section:
NCT01618305
Adverse Events Module:
NCT01618305