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Neonatal Catheter Lock for Infection Prevention

NCT07585188 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2026-10
Last updated
2026-05-13

Condition(s) studied

CLABSI - Central Line Associated Bloodstream InfectionCRBSI - Catheter Related Bloodstream InfectionNeonatal Sepsis, Late-Onset

Investigational drug(s) / intervention(s)

Taurolidine 2% lockNormal saline lock

Taurolidine 2% lock: Lock with a 2% taurolidine solution for a duration of 30 minutes every 48 hours, from CVC insertion until its removal, performed in newborns with epicutaneo-caval catheters (ECCs), femoral inserted central catheters (FICCs), or centrally inserted central catheters (CICCs).

Normal saline lock: Lock with normal saline for a duration of 30 minutes every 48 hours, from CVC insertion until its removal, performed in newborns with epicutaneo-caval catheters (ECCs), femoral inserted central catheters (FICCs), or centrally inserted central catheters (CICCs).

Study summary

For newborns admitted to Neonatal Intensive Care Units (NICUs), one of the main risk factors for late-onset sepsis is the presence of a central venous catheter (CVC), which is often essential for the administration of medications and parenteral nutrition in this patient population. From a nosological perspective, sepsis associated with the presence of a venous catheter is defined by two acronyms: CRBSI (Catheter-Related Bloodstream Infection - a microbiological definition) and CLABSI (Central Line-Associated Bloodstream Infection - an epidemiological definition).

Among preventive strategies for CRBSI/CLABSI, antibiotic or antimicrobial catheter lock solutions - instilled in a volume equivalent to the catheter dead space and retained within the lumen until the next use - have demonstrated favorable efficacy in reducing infection risk.

Taurolidine 2% is considered a preferred agent due to its broad-spectrum antibacterial and antifungal activity and its lack of association with the development of antimicrobial resistance.

However, its prophylactic use in neonates remains largely investigational, with current evidence limited to small, retrospective observational studies involving catheters ≥3 Fr (e.g., femoral inserted central catheters - FICCs, centrally inserted central catheters - CICCs, and umbilical venous catheters).

In NICUs, epicutaneo-caval catheters (ECCs) are the most commonly used central venous access devices and represent a major source of catheter-related infections. Despite this, the use of antimicrobial lock prophylaxis in ECCs has been limited by concerns regarding catheter occlusion, given their smaller diameter (≤2 Fr). Nevertheless, available evidence indicates that short-duration locks, when combined with meticulous infusion line management, can be safely implemented without increasing the risk of catheter occlusion.

The aim of the study is to evaluate the efficacy of 2% taurolidine lock in the prevention of CLABSI/CRBSI in neonates with CVC (ECC, FICC, or CICC).

Eligibility

Sex
ALL
Min age
1 Day
Max age
120 Days
Healthy volunteers
No
Inclusion Criteria: * presence of a CVC (ECC, CICC, or FICC) for at least 48 hours * absence of systemic antibiotic therapy in the 48 hours preceding enrollment Exclusion Criteria: * presence of an umbilical venous catheter * suspected thrombophilic disorder

Primary outcome measure(s)

  • Incidence of CLABSI episodes expressed as events per 1000 catheter-days — From first catheter lock intervention until removal of all central venous catheters (CVCs), an average of 14 days

Trial sites (1)

FacilityCityRegionStatus
Sant'Anna Hospital, University of Turin Turin Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07585188 on ClinicalTrials.gov ↗ ← All trials in Italy