Study Results
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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UNKNOWN
NA
280 participants
INTERVENTIONAL
2020-06-15
2023-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Experimental : Cannulation with AccuVein AV400
Cirrhotic patients benefit from the support of a venous illumination device for each peripheral venous cannulation
Cannulation with AccuVein AV400
Cannulation using AccuVein AV400 device
Control
Cirrhotic patients benefit from the standard technique of peripheral veinous catheter placement.
No interventions assigned to this group
Interventions
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Cannulation with AccuVein AV400
Cannulation using AccuVein AV400 device
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patient presenting a liver cirrhosis
* Patient requiring the placement of a venous peripheral catheter
* Patient informed and giving free and informed consent
* Patient affiliated to a French social security scheme
Exclusion Criteria
* Patient unable to give consent
* Patient under guardianship or curatorship
18 Years
ALL
No
Sponsors
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University Hospital, Caen
OTHER
Responsible Party
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Locations
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Caen University Hospital
Caen, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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19-043
Identifier Type: -
Identifier Source: org_study_id
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