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Clinical Trials/NCT02894073
NCT02894073
Unknown
Not Applicable

Interest of a Skin Transilluminator (Such as the VeinViewer®Vision Device) for Peripheral Venous Catheter Placement in the Obese Patient: a Randomized, Controlled Pilot Study

Centre Hospitalier Universitaire, Amiens1 site in 1 country2 target enrollmentMarch 21, 2017
ConditionsGeneral Surgery

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
General Surgery
Sponsor
Centre Hospitalier Universitaire, Amiens
Enrollment
2
Locations
1
Primary Endpoint
duration of the PVC placement procedure
Last Updated
7 years ago

Overview

Brief Summary

Placement of a peripheral venous catheter (PVC) is the most common invasive procedure in anaesthesia and perhaps even in the field of medicine as a whole.

Detailed Description

Placement of a peripheral venous catheter (PVC) is the most common invasive procedure in anaesthesia and perhaps even in the field of medicine as a whole. This procedure may be challenging in the obese patient - even for the most experienced healthcare professionals. In a study, PVC placement was considered to be difficult in 46% of obese patients but only 13% of non-obese patients. Placement of a central venous catheter is an option when PVC placement is impossible, although central access is associated with a non-negligible risk of complications (pneumothorax, infection, arterial puncture, etc.). Facilitating peripheral venous access in obese patients should shorten the time required for PVC placement, decrease the number of perfusion attempts (a source of dissatisfaction and discomfort for the patients) and limit the use of a central venous catheter. Although a number of novel vein visualisation devices (such as the VeinViewer®Vision from Christie Medical) have been developed to guide PVC placement, there are no literature data on the value of these devices in the management of difficult venous access in obese patients.

Registry
clinicaltrials.gov
Start Date
March 21, 2017
End Date
August 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All obese adult patients scheduled for surgery.
  • Social security coverage

Exclusion Criteria

  • Contra-indication to PVC placement.
  • Legal guardianship.

Outcomes

Primary Outcomes

duration of the PVC placement procedure

Time Frame: Day 0

the time between the first puncture and the confirmation of successful PVC placement via the injection of physiological saline

Study Sites (1)

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