Evaluation of Accuvein in Obese Patients

Primary Care Clinical Trial

— AVO  

Official title:

Evaluation of Accuvein in Obese Patients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02015845
• Other study ID #: 2013/19
• Secondary ID: 2013-A00777-38
• Status: Terminated
• Phase: N/A
• First received: December 5, 2013
• Last updated: May 18, 2017
• Start date: November 2013
• Est. completion date: May 2017

Study information

• Verified date: May 2017
• Source: Hopital Foch
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to evaluate the effectiveness of Accuvein to facilitate placement of peripheral intravenous catheters in obese patients. This clinical protocol is designed to determine whether using Accuvein increases the ease and efficiency of venous cannulation (as perceived by the operator), decreases the time to effective cannulation, and decreases the patient's perception of the pain.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 26
• Est. completion date: May 2017
• Est. primary completion date: May 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• obese adults ( BMI equal or greater 35) requiring a venous blood sampling or the placement of a venous peripheral catheter

Exclusion Criteria:

• pregnant woman

Related Conditions & MeSH terms

• Primary Care

Intervention

Device:
• Accuvein

• Routine technique
Placement of peripheral intravenous catheters using the routine technique

Locations

Country	Name	City	State
France	Institut Hospitalier Franco-Britannique	Levallois-Perret	Hauts de Seine

Sponsors (1)

Lead Sponsor	Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of success of the first vein puncture	Successful successful placement of IV catheter	one hour
Secondary	Score of evaluation of the device	Evaluation of the device by the operator and the patient	one hour