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Closed-blood Sampling Devices in the Adult Critically Ill Patient

RecruitingNAAges 18 Years - anyAllUniversity of Barcelona
NCT06478160 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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practice (waste discard volume, control group), in critically ill adult patients, will decrease the amount of blood withdrawn for laboratory tests, we want to analyze the number of red blood cells (RBC) administered and arterial catheter-related adverse events (catheter-related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.

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📋 Eligibility rules (as published)
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.
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What it tests

  • Closed-Blood Sampling Devices
  • Waste discard volume
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Where

3 sites
Hospital Universitario 12 de Octubre
Madrid, Spain
Hospital Rey Juan Carlos
Madrid, Spain
Hospital Virgen de la Macarena
Seville, Spain
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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