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Clinical Trial Summary

The purpose of this investigation is to conduct a randomized, patient-blinded prospective controlled trial comparing peripheral intravenous cannulation in children done by:

1. Conventional landmark cannulation where the intravenous cannulation is done by direct visual guidance or palpation or a combination thereof.

2. Ultrasound guided cannulation by means of DNTP.

The investigators hypothesize that with ultrasound-guided peripheral intravenous cannulation the first-attempt success rate will be significantly higher than by the conventional landmark cannulation technique.


Clinical Trial Description

n/a


Study Design

Intervention Model: Crossover Assignment, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT02556541
Study type Interventional
Source University of Aarhus
Contact Nigopan Gopalasingam
Phone +45 31535950
Email 20103907@post.au.dk
Status Recruiting
Phase N/A
Start date September 2015

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