Clinical Trials Directory

Trials / Terminated

TerminatedNCT03675711

Midline Catheter and Its Impact on Central Lines Removal in ICU

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
83 (actual)
Sponsor
Centre Hospitalier Departemental Vendee · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study will evaluate 2 strategies to remove central venous catheter (CVC): in one part, the insertion of a midline catheter and in the other part, the conventional insertion of peripheral venous catheter (PVC)

Detailed description

Patients will be randomised when the last indication for CVC has disappeared, which means parenteral nutrition or vasopressors administration. They will be randomised either in the midline group or in the PVC group. * In the midline group, a midline catheter will try to be inserted before the 48th hour after last indication for CVC disappeared. * In the PVC group: a PVC will try to be inserted before the 48th hour after last indication for CVC disappeared. If successful, CVC will then be removed. If not, a PVC will try to be inserted daily till success or worthlessness of a venous line or death. The presence of a CVC will be assessed at the 96th hour after disappearance of last CVC indication.

Conditions

Interventions

TypeNameDescription
DEVICEMidlinePatient will receive a Midline catheter within 48h after disappearance of indication for CVC
DEVICEPVCPatient will receive a standard PVC within 48h after disappearance of indication for CVC

Timeline

Start date
2018-11-02
Primary completion
2023-01-03
Completion
2023-01-13
First posted
2018-09-18
Last updated
2023-03-22

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03675711. Inclusion in this directory is not an endorsement.