Closed-blood Sampling Devices in the Adult Critically Ill Patient

NCT06478160 · tracked via the Priya Life Science Spain tracker

Sponsor

University of Barcelona

Phase

Not applicable

Started

2024-11-11

Last updated

2025-11-10

Condition(s) studied

Acceptability of Health Care

Investigational drug(s) / intervention(s)

Closed-Blood Sampling DevicesWaste discard volume

Closed-Blood Sampling Devices: blood collection with Closed-Blood Sampling System (CBSD)

Waste discard volume: Blood collection without CBSD, usual practice, need to waste discard volume

Study summary

Based on the hypothesis that the strategy of using Closed-Blood Sampling Devices (CSBD, experimental group) compared to the usual practice (waste discard volume, control group), in critically ill adult patients, will decrease the amount of blood withdrawn for laboratory tests, we want to analyze the number of red blood cells (RBC) administered and arterial catheter-related adverse events (catheter-related bacteremia, catheter obstruction, CBSD malfunction, loss of arterial pressure waveform on the patient's bedside monitor) in both study groups, during ICU stay and up to a maximum of 21 days.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Adult patients with an arterial catheter who agree to participate in the study, with a stay in the ICU of 24h and a minimum of 72h more with an arterial catheter Non-inclusion criteria: Therapeutic Limitation of Life Support, Jehovah's Witnesses. Exclusion Criteria: * Patients with chronic renal failure * Patients with active gastrointestinal bleeding * Patients diagnosed with hematologic cancer * Women with menstruation at the time of admission * Pregnant women Withdrawal criteria: presence of active gastrointestinal bleeding during the study inclusion period.

Primary outcome measure(s)

Units of red blood cells transfusion — Every day during the ICU stay and up to a maximum of 21 days after randomization (day 0)
Number of red blood cells (RBC) units administered in both study groups

Trial sites (3)

Facility	City	Region	Status
Hospital Universitario 12 de Octubre	Madrid	Madrid	Completed
Hospital Rey Juan Carlos	Madrid	Madrid	Recruiting
Hospital Virgen de la Macarena	Seville	Sevilla	Recruiting

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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 NCT06478160 on ClinicalTrials.gov ↗ ← All trials in Spain