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Evaluation of Accuvein in Adult Patients

NCT01020461 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 522

Last updated 2016-09-23

No results posted yet for this study

Summary

The objective of this study is to evaluate the effectiveness of Accuvein to facilitate venous blood sampling and placement of peripheral intravenous catheters in adults. 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, decreases the number of sticks, and decreases the patient's perception of the pain.

Conditions

  • Catheterization

Interventions

DEVICE

Accuvein

Accuvein will be used to facilitate venous blood sampling

DEVICE

Accuvein

Accuvein will be used to facilitate peripheral IV catheter placement

Sponsors & Collaborators

  • Hopital Foch

    lead OTHER

Principal Investigators

  • Marc Fischler, MD · Hôpital Foch

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01020461 on ClinicalTrials.gov