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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03555864
Other study ID # Local-PC-2017-2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 6, 2017
Est. completion date July 4, 2019

Study information

Verified date July 2019
Source Centre Hospitalier Universitaire de Nimes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Peripheral venous access is a prerequisite for anesthesiological for surgical patients.It is often difficult to establish and potentially painful in obese patients (Body mass Index > 35). AV300 uses near infrared laser light to improve visibility of peripheral veins and could help cannulating them. The aim of this study was to examine if use of Accuvein(®) AV300 vein viewer could facilitate venous cannulation in obese patients (surgical and obstetric).


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date July 4, 2019
Est. primary completion date November 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria

- > 18 years

- surgery that need double intravenous perfusion

Exclusion Criteria:

- < 18 years

- body mass index< 35

- refusal

- minor surgery that need only one intravenous access

Study Design


Related Conditions & MeSH terms


Intervention

Device:
infrared transluminescent device
use of infra red for venous access for second intravenous access

Locations

Country Name City State
France CHU Nimes Nîmes Gard

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary success for second intravenous line using infra red number of attempts 1 day
Secondary time time in second for second intravenous access 1 day
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