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Evaluation of a new vessel imaging system to support venous cannulation in children prior to elective, non-cardiac surgery in patients with a dark skin color.

Evaluation of a new vessel imaging system to support venous cannulation in children prior to elective, non-cardiac surgery in patients with a dark skin color.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23953
Enrollment
110
Registered
2011-09-05
Start date
2011-01-01
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

Infrared, Venous cannulation, Vessel visualization, Venipuncture

Interventions

The VascuLuminator is the investigational product in this study. It is able to non-invasively visualize blood vessels by means of near-infrared light. The intervention consists of the use of the devic

Sponsors

University Medical Center Utrecht (UMCU)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consecutive patients aged less than 18 years, undergoing elective, non-cardiac surgery in a primary general hospital at Curacao in the Caribbean will be included in the present trial.

Exclusion criteria

Exclusion criteria: N/A

Design outcomes

Primary

MeasureTime frame
The main study parameter is success at first attempt (defined as the percentage of procedures in which the venous cannulation succeeded at the first attempt. An attempt is a penetration with a needle through the skin.)

Secondary

MeasureTime frame
1. Number of punctures; 2. Time to successful cannulation, if the procedure succeeded or not and if the VL was helpful or not. Timing starts at the moment the first attempt is made to search for a suitable vessel, by palpating or looking (with the system in use, looking with the system) and ends at the moment the line is flushed.

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)