Using the Accuvein Device for Patients Who Are Difficult to Perfuse

Condition(s) studied

Investigational drug(s) / intervention(s)

accuvein: intravenous route with accuvein

with out accuvein: intravenous route with out accuvein

Study summary

Prior to any examination related to the clinical investigation, the investigator (IDE) will check the eligibility criteria of the person undergoing the research, and will inform and obtain the free, informed and written consent of the person undergoing the research.

The patient will then be randomised into one of two groups (insertion of a intravenous route with the AccuVein device vs. insertion of a VVP without the AccuVein device). After randomisation, the TEC or qualified person starts the stopwatch as soon as the tourniquet is applied.

The nurse makes a first attempt to perfuse the patient. The TEC or the qualified person will stop the stopwatch when the nurse checks the patency of the first attempt at perfusion and signals its success, or when the nurse withdraws the needle if the first attempt is unsuccessful. The pain felt by the patient will be assessed by the nurse using the self-assessment scale from 0 to 10 at the end of the first attempt.

If the first attempt at VVP insertion fails, the choice of conditions and personnel involved in carrying out further attempts will be left to the discretion of the nurse.

Eligibility

Primary outcome measure(s)

• Successful first attempt at intravenous route insertion defined by a functional perfusion placed in a vein — day 1

Trial sites (1)

More University Hospital, Rouen trials in France