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 @ 4:19 PM
Ignite Modification Date:
2025-12-25 @ 2:16 PM
NCT ID:
NCT01659866
Group ID:
EG001
Title:
Cipro-resistant
Description:
Patients with ciprofloxacin-resistant bacteria on their rectal swab will receive one of the following drugs:
* trimethoprim-sulfamethoxazole 1 double strength tablet orally 2 hours before the procedure and again 12 hours later
* cefuroxime 500 mg orally 2 hours before the procedure then again 12 hours later
* ceftriaxone 500 mg intramuscularly 2 hours before the procedure
* gentamicin 2mg/kg intramuscularly 2 hours before the procedure
* amikacin 5 mg/kg intramuscularly 2 hours before the procedure
* aztreonam 500 mg intramuscularly 2 hours before the procedure
* imipenem 500 mg intramuscularly 2 hours before the procedure
* ceftriaxone 2000 mg intravenously 1 hour before the procedure
* gentamicin 2 mg/kg intravenously 1 hour before the procedure
* amikacin 5mg/kg intravenously 1 hour before the procedure
* aztreonam 2000 mg intravenously 1 hour before the procedure
* imipenem 1000 mg intravenously 1 hour before the procedure
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
80
Other Number Affected:
0
Other Number At Risk:
80
Study:
NCT01659866
Results Section:
NCT01659866
Adverse Events Module:
NCT01659866