Peripheral IV study: Data Sheet, Study Flow, Data Collection Tips, FAQs
 

Overview:  This study seeks to determine the rate of complications resulting from IV starts in the ED.
 

Endpoints: Patient report of signs of infection or complications.
 

Eligible Patients: Patients who are over 18 yo who have received an IV.
 

Study Design: Prospective observational trial
 

Anticipated Benefits: none
 

Potential Risks: none
 

Research Associate’s Role: RA’s are responsible for collecting data on patients enrolled into the study.
 

Physician’s Role: Same as RA.
 

Location of Study Packets: TCA, TCB, TCC