Development and Evaluation of an Algorithm for Vascular Access Management

Recruiting N/A Interventional Study
Peripheral Venous Access
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
794 (estimated)
Sponsor
Central Hospital, Nancy, France · Other
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About This Trial
Two billion catheters are placed annually worldwide. Of all the people requiring vascular access, nearly a quarter have Difficult Intravenous access (DIVA), a source of multiple punctures. The increased risk of haematomas, haemorrhages, infection, pain and associated trauma is responsible for increased human costs and economic impact. To limit the risks posed by the DIVA, practitioners have solut…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient inclusion criteria: adult patients, initially requiring at least one peripheral venous catheter (PVC), having given their consent for the study. * Inclusion criteria for healthcare professionals: Nurses, specialized nurses (IADE) and physicians attached to the departme…
Contacts

Amandine OSTERMANN

03 83 85 28 52

a.ostermann@chru-nancy.fr

CONTACT

Côme SLOSSE

c.slosse@chru-nancy.fr

CONTACT