Evaluation of Accuvein in Obese Patients

Not Applicable

Terminated

• Conditions: Primary Care
• Interventions: Device: Accuvein; Device: Routine technique

• Registration Number: NCT02015845
• Lead Sponsor: Hopital Foch

Brief 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.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-11
• Study First Submitted: 2013-12-05
• Study First Submitted QC: 2013-12-13
• Study First Posted: 2013-12-19
• Status Verified: 2017-05
• Primary Completion: 2017-05
• Study Completion: 2017-05
• Last Update Submitted: 2017-05-18
• Last Update Posted: 2017-05-19

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

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

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Exclusion Criteria

• pregnant woman

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Accuvein	Accuvein	Use of Accuvein to facilitate placement of peripheral intravenous catheters in obese patients
Routine technique	Routine technique	Routine technique used to insert a peripheral intravenous catheters in obese patients.

Primary Outcome Measures

Name	Time	Method
Percentage of success of the first vein puncture	one hour	Successful successful placement of IV catheter

Secondary Outcome Measures

Name	Time	Method
Score of evaluation of the device	one hour	Evaluation of the device by the operator and the patient

Trial Locations

Locations (1)

Institut Hospitalier Franco-Britannique; 🇫🇷 Levallois-Perret, Hauts de Seine, France