Evaluation of Accuvein in Adult Patients

Hopital Foch

Status and phase: Terminated; Phase 4

Conditions: Catheterization

Treatments: Device: Accuvein

Study type: Interventional

Funder types: Other

Identifiers

NCT01020461

2009/43

Details and patient eligibility

About

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.

Enrollment: 522 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• none

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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522 participants in 2 patient groups

Venous blood sampling

Experimental group

Description:

To use Accuvein to improve the effectiveness of venous blood sampling

Treatment:

Device: Accuvein

Device: Accuvein

Peripheral IV catheter placement

Experimental group

Description:

To use Accuvein to improve the effectiveness of placing peripheral IV catheter

Treatment:

Device: Accuvein

Device: Accuvein