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Ultrasound-guided Peripheral Vascular Access in Children

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ClinicalTrials.gov Identifier: NCT02556541
Recruitment Status : Unknown
Verified April 2015 by University of Aarhus.
Recruitment status was:  Recruiting
First Posted : September 22, 2015
Last Update Posted : March 7, 2016
Sponsor:
Information provided by (Responsible Party):
University of Aarhus

Brief 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.


Condition or disease Intervention/treatment Phase
Ultrasonography Vascular Access Devices Pediatrics Procedure: IV puncture guided by ultrasound Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Intervention Model: Crossover Assignment
Primary Purpose: Supportive Care
Official Title: Ultrasound-guided Peripheral Vascular Access in Children - a Single- Blind, Randomized, Cross-over Trial
Study Start Date : September 2015
Estimated Primary Completion Date : August 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Ultrasound




Primary Outcome Measures :
  1. First attempt success [ Time Frame: Intraoperative ]
    Succes rate of first attempt cannulation for ultrasound and traditional method will be compared.



Information from the National Library of Medicine

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Ages Eligible for Study:   up to 3 Years   (Child)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  • Requirement for anaesthesia before MRI or operation.
  • Routine need of peripheral intravenous cannulation.
  • Age 0- 3 years at the date of MR scan

Exclusion Criteria:

  • Lack of consent
  • Emergency patients needing immediate operation or scan.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02556541


Contacts
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Contact: Nigopan Gopalasingam +45 31535950 20103907@post.au.dk

Locations
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Denmark
Department of Anaesthesiology and Intensive Care Recruiting
Aarhus, Denmark, 8200
Contact: Erik Sloth, professor, phd, MD    78 45 10 28    sloth@dadlnet.dk   
Sponsors and Collaborators
University of Aarhus
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Responsible Party: University of Aarhus
ClinicalTrials.gov Identifier: NCT02556541    
Other Study ID Numbers: 1-10-72-94-15
First Posted: September 22, 2015    Key Record Dates
Last Update Posted: March 7, 2016
Last Verified: April 2015