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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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22 April 2013 |
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Main ID: |
NCT01020461 |
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Date of registration:
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22/11/2009 |
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Primary sponsor: |
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Public title:
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Evaluation of Accuvein in Adult Patients
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Scientific title:
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Evaluation of Accuvein for Blood Sampling and for Intravenous Catheter Placement in Adult Patients |
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Date of first enrolment:
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January 2010 |
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Target sample size:
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522 |
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Recruitment status: |
Terminated |
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URL:
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http://clinicaltrials.gov/show/NCT01020461 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Countries of recruitment
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France
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Contacts
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Name:
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Marc Fischler, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Hôpital Foch |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- adults requiring a venous blood sampling or the placement of a venous peripheral
catheter
Exclusion Criteria:
- none
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Catheterization
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Intervention(s)
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Device: Accuvein
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Primary Outcome(s)
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Time to successful blood sampling or to successful placement of IV catheter
[Time Frame: one hour]
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Secondary Outcome(s)
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Increases in the ease and efficiency of venous cannulation perceived by the operator)
[Time Frame: Immediately after attempts]
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Number of attempts required
[Time Frame: Immediately after attempts]
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Pain
[Time Frame: Immediately after attempts]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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