← Eichor
Study identifier: NCT06656104 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Impact of a Multi-infusion Strategy in Neonatology on the Rate of Central Line-associated Bloodstream Infections

Condition: Neonatal Infection  ·  Sponsor: Hospices Civils de Lyon

PhaseN/A
Planned participants455
Who can joinAll sexes, N/A to 32 Weeks
Healthy volunteersNo

About this study

The management of premature infants hospitalized in neonatal units requires the simultaneous intravenous (IV) infusion of several drugs and parenteral nutrition solutions, when oral administration is impossible or unsuitable. IV administration requires the use of a central venous catheter and an infusion set that connects the catheter to the infusion fluid or drug. The use of multiple infusion devices exposes patients to central line-associated bloodstream infections (CLABSI), drug interactions, abnormal administration timing and repetition of procedures in close proximity to the infant. Against this backdrop, DORAN INTERNATIONAL has developed the EDELVAISS multi-infusion strategy (Multiline Neo® and Escape Line® devices) adapted to neonatology. Given its characteristics, the benefits expected from the use of this strategy are: 1) to reduce the risk of microbial contamination and therefore the number of nosocomial infections 2) reduce exposure to antibiotics used in late sepsis 3) reduce the number of central line losses due to catheter obstruction 4) reduce dys-stimulating procedures in contact with the infant and 5) reduce staff stress. A pilot study before (year 2019) and after (year 2020) was carried out in the tertiary care neonatal unit at Croix-Rousse hospital. The baseline CLABSI rate was slightly below the national level of the last French survey (12.4/1000 catheter days \[95%CI:10.8;14.0\]). In 322 very-low-birth-weight infants, the investigators showed a signific…

This description comes directly from the study's public registry record.

Talk to the study team

Jean-Charles PICAUD, MD, PhD  ·  04 72 00 15 50  ·  jean-charles.picaud@chu-lyon.fr

Fanny JOUBERT  ·  04 26 73 27 27  ·  fanny.joubert@chu-lyon.fr

Always discuss trial participation with your own doctor first.

Locations (3)

Service de néonatologie Hôpital Femme Mère EnfantBron, France, FranceRecruiting
Service Pédiatrie néonatale et réanimations CHU MontpellierMontpellier, France, FranceNot Yet Recruiting
Service de néonatologie CHU de StrasbourgStrasbourg, France, FranceActive Not Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06656104