Supporting intravenous cannulation in children with infrared light; A clinical evaluation of three systems.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON27576

Enrollment

1000

Registered

2010-12-20

Start date

2011-01-12

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Vessel visualization, Venipuncture, VascuLuminator, Infuus, Venous cannulation, Accuvein, Veinviewer, succes rate

Interventions

The study consists of four arms: Three arms with one of the devices (the Accuvein, Veinviewer or the VascuLuminator) and one control arm with the standard procedure of intravenous cannulation. When on

Eligibility

Inclusion criteria

Inclusion criteria: All consecutive patients aged less than 18 years, scheduled for elective surgery.

Exclusion criteria

Exclusion criteria: Patients with a canula already in situ.

Design outcomes

Primary

Measure	Time frame
To evaluate the effectivity of three different devices developed to visualize blood vessels with light, in intravenous cannulation in children.	—

Secondary

Measure	Time frame
To investigate if the devices are able to visualize blood vessels in the study population.	—

Contacts

Public ContactNatascha Cuper

Mailstop C.01.230 P.O. Box 85500

n.j.cuper@umcutrecht.nl+31(0)88 755 3243

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)