Evaluation of Accuvein in Obese Patients

NCT ID: NCT02015845

Last Updated: 2017-05-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-11-30

Study Completion Date

2017-05-31

Brief Summary

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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

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Conditions

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Primary Care

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Accuvein

Use of Accuvein to facilitate placement of peripheral intravenous catheters in obese patients

Group Type EXPERIMENTAL

Accuvein

Intervention Type DEVICE

Routine technique

Routine technique used to insert a peripheral intravenous catheters in obese patients.

Group Type ACTIVE_COMPARATOR

Routine technique

Intervention Type DEVICE

Placement of peripheral intravenous catheters using the routine technique

Interventions

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Accuvein

Intervention Type DEVICE

Routine technique

Placement of peripheral intravenous catheters using the routine technique

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hopital Foch

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Institut Hospitalier Franco-Britannique

Levallois-Perret, Hauts de Seine, France

Site Status

Countries

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France

Other Identifiers

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2013-A00777-38

Identifier Type: OTHER

Identifier Source: secondary_id

2013/19

Identifier Type: -

Identifier Source: org_study_id

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