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Evaluation of Accuvein in Adult Patients

Evaluation of Accuvein for Blood Sampling and for Intravenous Catheter Placement in Adult Patients

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01020461
Enrollment
522
Registered
2009-11-25
Start date
2010-01-31
Completion date
2013-04-30
Last updated
2016-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Catheterization

Brief summary

The objective of this study is to evaluate the effectiveness of Accuvein to facilitate venous blood sampling and placement of peripheral intravenous catheters in adults. This clinical protocol is designed to determine whether using Accuvein increases the ease and efficiency of venous cannulation (as perceived by the operator), decreases the time to effective cannulation, decreases the number of sticks, and decreases the patient's perception of the pain.

Interventions

DEVICEAccuvein

Accuvein will be used to facilitate venous blood sampling

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adults requiring a venous blood sampling or the placement of a venous peripheral catheter

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
Time to successful blood sampling or to successful placement of IV catheterone hour

Secondary

MeasureTime frame
Number of attempts requiredImmediately after attempts
PainImmediately after attempts
Increases in the ease and efficiency of venous cannulation perceived by the operator)Immediately after attempts

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026