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Ultrasound-guided Peripheral Vascular Access in Children

Sponsor
University of Aarhus (Other)
Overall Status
Unknown status
CT.gov ID
NCT02556541
Collaborator
(none)
50
Enrollment
1
Location

Study Details

Study Description

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
  • Procedure: IV puncture guided by ultrasound
 N/A

Study Design

Study Type:
Interventional
Anticipated 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 :
Sep 1, 2015
Anticipated Primary Completion Date :
Aug 1, 2016

Outcome Measures

Primary Outcome Measures

  1. First attempt success [Intraoperative]

    Succes rate of first attempt cannulation for ultrasound and traditional method will be compared.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 3 Years
Sexes Eligible for Study:
All
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Anaesthesiology and Intensive Care Aarhus Denmark 8200

Sponsors and Collaborators

  • University of Aarhus

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT02556541
Other Study ID Numbers:
  • 1-10-72-94-15
First Posted:
Sep 22, 2015
Last Update Posted:
Mar 7, 2016
Last Verified:
Apr 1, 2015

Study Results

No Results Posted as of Mar 7, 2016