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Starting soon Observational

Air-in-Line Alarms During Antineoplastic Drug Infusion

NCT07718711 · tracked via the Priya Life Science Italy tracker
Sponsor
Associazione Italiana Infermieri di Area Oncologica
Phase
Observational
Started
2026-07-01
Last updated
2026-07-22

Condition(s) studied

Infusion SafetyMedication SafetyAntineoplastic Drug AdministrationAir-in-Line Alarm

Investigational drug(s) / intervention(s)

Routine Infusion Technologies

Routine Infusion Technologies: Observation of routinely used infusion technologies and infusion-related alarm management during standard antineoplastic drug administration in oncology care settings. No experimental intervention or treatment allocation is performed.

Study summary

The goal of this observational study is to evaluate infusion alarms, particularly air-in-line alarms, during antineoplastic drug infusion in oncology care settings.

The main questions it aims to answer are:

How frequently do infusion alarms occur, and what types of alarms are observed during antineoplastic drug infusion? How long does it take healthcare professionals to manage infusion alarms and restore infusion continuity? What strategies do healthcare professionals use to manage infusion alarms? How do healthcare professionals evaluate the user experience of different infusion technologies?

Participants will be healthcare professionals involved in antineoplastic drug infusion. They will not receive any experimental intervention. Researchers will observe routine infusion procedures and collect data on alarm events, alarm management, infusion technologies, and user experience.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Healthcare professionals involved in the administration of antineoplastic drugs in participating oncology centres. * Employment in a participating study site during the study period. * Direct involvement in routine intravenous antineoplastic drug infusion procedures. * Participation in infusion procedures eligible for observation according to the study protocol. Exclusion Criteria: * Healthcare professionals not directly involved in antineoplastic drug administration. * Healthcare professionals working outside participating study sites. * Temporary staff not routinely involved in infusion activities during the observation period. * Refusal to participate in study activities where local regulations require participant notification.

Primary outcome measure(s)

  • Frequency and Type of Infusion Alarms — Up to 24 months
    Number and type of infusion alarms, including air-in-line alarms, recorded during simulated and real-world antineoplastic infusion procedures.

Trial sites (5)

FacilityCityRegionStatus
AUSL Parma Parma Emilia-Romagna
Fondazione Policlinico Universitario A. Gemelli IRCCS Rome Lazio
ASST Lodi Lodi Lombardy
IRCCS Ospedale San Raffaele Milan Lombardy
IEO - Istituto Europeo di Oncologia Milan Lombardy
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 NCT07718711 on ClinicalTrials.gov ↗ ← All trials in Italy