Clinical Trials Directory

Trials / Terminated

TerminatedNCT01020461

Evaluation of Accuvein in Adult Patients

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

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
522 (actual)
Sponsor
Hopital Foch · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEAccuveinAccuvein will be used to facilitate venous blood sampling
DEVICEAccuveinAccuvein will be used to facilitate peripheral IV catheter placement

Timeline

Start date
2010-01-01
Primary completion
2013-04-01
Completion
2013-04-01
First posted
2009-11-25
Last updated
2016-09-23

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01020461. Inclusion in this directory is not an endorsement.

Evaluation of Accuvein in Adult Patients (NCT01020461) · Clinical Trials Directory