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 @ 5:08 AM
Ignite Modification Date:
2025-12-26 @ 4:12 AM
NCT ID:
NCT03161327
Group ID:
EG000
Title:
ABIABI Using QuantaFlo™
Description:
ABI will be performed in patient
ABI using QuantaFlo™: Perform Digital ABI:
* Will be performed by the nurse/medical assistant with training to perform this test
* The patient will be placed in the supine position, with the arms and legs at the same level as the heart, for a minimum of 5 minutes before measurement.
* The optical sensor (similar to a pulse oximeter) will be placed sequentially in the fingers of the hands and feet: Right and left hand fingers and then right and left feet toes.
* Usually each digit takes about 15 seconds to obtain a waveform
* At the end of 60 seconds, an automated digital ABI will be generated.
Clinical course: If based on Screening questionnaire and digital ABI, I. Patient is diagnosed with PAD- the referring physician and patient will receive a phone call about the same. He/ she will then be advised any further testing/ referral to IR clinic.
II. There is no evidence of PAD- no further action will be taken. The patient will be informed
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
238
Other Number Affected:
0
Other Number At Risk:
238
Study:
NCT03161327
Results Section:
NCT03161327
Adverse Events Module:
NCT03161327