Actively Recruiting
Impact of Infusion Line Change Frequency on Infectious Complications Related to Central Venous Catheters in the ICU - A Randomized Controlled Trial
Led by University Hospital, Angers · Updated on 2026-05-13
2830
Participants Needed
27
Research Sites
133 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In the intensive care unit, patients' care and secure drugs administration require a central venous catheter. These invasive devices can lead to complications, particularly infections. Most preventive recommendations focus on catheter insertion, line handling, and dressings. Few recommendations adress catheter dwell time, which is certainly the main source of infection. Part of the prevention strategy is the regular and systematic replacement of infusion sets , as they may become contaminated during use, mainly through the hands of healthcare professionals. Prolonged use increases the risk of infection. Infusion lines changes involve disconnecting the old sets, discarding infusion devices containing drug residues, and replacing them with new sterile devices. Current international guidelines recommend replacing these sets every 4 days, and the Center for Disease Control and Prevention recommends not exceeding 7 days. Replacing these devices requires the time of qualified nurses, numerous sterile medical devices, and medications. In addition to the intended effect on infection prevention, the procedure has impacts on workload and costs. The objective of the study is to demonstrate that changing infusion set every 7 days does not increase the rate of central venous catheters related infections compared with changing infusion set every 4 days.
CONDITIONS
Official Title
Impact of Infusion Line Change Frequency on Infectious Complications Related to Central Venous Catheters in the ICU - A Randomized Controlled Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient
- Any ICU patient with a central venous catheter inserted by venipuncture in place for less than 72 hours
- Expected catheter dwell time of at least 7 days
- Patient covered by a social security system
- Patient has given verbal consent or written consent from a third party if unable to consent
You will not qualify if you...
- Documented bloodstream infection at the time of inclusion
- Central venous catheter in place for more than 72 hours
- Suspected catheter-related infection
- Catheter inserted using a guidewire exchange
- Previously enrolled in the study during the same ICU stay
- Condition preventing safe catheter placement, including allergy to catheter material, confirmed deep vein thrombosis, or inflammatory skin disorder at insertion site
- Admitted for extensive burns
- Inadequate understanding of French language
- Pregnant, breastfeeding, or postpartum woman
- Person deprived of liberty by judicial or administrative decision
- Person receiving involuntary psychiatric care
- Person under legal guardianship or other legal protection measure
AI-Screening
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Trial Site Locations
Total: 27 locations
1
La Réunion University Hospital
Saint-Pierre, La Réunion, France, BP350 97448
Not Yet Recruiting
2
Albi Hospital
Albi, France, 81000
Not Yet Recruiting
3
Angers University Hospital
Angers, France, 49933
Actively Recruiting
4
Belfort Hospital
Belfort, France, 90015
Not Yet Recruiting
5
Bourges Hospital
Bourges, France, 18000
Not Yet Recruiting
6
Caen University Hospital
Caen, France, 14033
Not Yet Recruiting
7
CH Carcassonne
Carcassonne, France, 11000
Not Yet Recruiting
8
Chartres Hospital
Chartres, France
Not Yet Recruiting
9
Cholet Hospital
Cholet, France, 49300
Not Yet Recruiting
10
Colombes Hospital
Colombes, France, 92700
Not Yet Recruiting
11
Corbeil-Essonnes Hospital
Corbeil-Essonnes, France, 91106
Not Yet Recruiting
12
AP-HP - Henri Mondor Hospital
Créteil, France, 94000
Not Yet Recruiting
13
Dijon University Hospital
Dijon, France, 21079
Not Yet Recruiting
14
Garches Hospital
Garches, France
Not Yet Recruiting
15
CH Le Mans
Le Mans, France, 72000
Not Yet Recruiting
16
Le Puy en Velay Hospital
Le Puy-en-Velay, France, 43000
Not Yet Recruiting
17
Macon Hospital
Mâcon, France, 71000
Not Yet Recruiting
18
Nantes University Hospital
Nantes, France, 44093
Not Yet Recruiting
19
Orleans University Hospital
Orléans, France, 45067
Not Yet Recruiting
20
AP-HP - Tenon Hospital
Paris, France, 75020
Not Yet Recruiting
21
AP-HP - Saint Louis
Paris, France, 75475
Not Yet Recruiting
22
Pontoise Hospital
Pontoise, France, 95300
Not Yet Recruiting
23
CHU Rennes - service MIR
Rennes, France, 35033
Not Yet Recruiting
24
CHU Rennes - service Réa chir
Rennes, France, 35033
Not Yet Recruiting
25
CH Saint-Nazaire
Saint-Nazaire, France, 44606
Not Yet Recruiting
26
Strasbourg University Hospital
Strasbourg, France, 67091
Not Yet Recruiting
27
CHU Tours
Tours, France, 37000
Not Yet Recruiting
Research Team
C
Carole Haubertin
CONTACT
A
Aurélie Hautefort
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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