Effectiveness of Closed-blood Sampling Devices in the Adult Critically Ill Patient: Multicenter Randomized Clinical Trial

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other, Device
Study Type: Interventional
Study Phase: Not Applicable
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practice (waste discard volume, control group), in critically ill adult patients, will decrease the amount of blood withdrawn for laboratory tests, we want to analyze the number of red blood cells (RBC) administered and arterial catheter-related adverse events (catheter-related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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Spain
Hospital Rey Juan Carlos
RECRUITING
Madrid
Hospital Universitario 12 de Octubre
COMPLETED
Madrid
Hospital Virgen de la Macarena
RECRUITING
Seville
Contact Information
Primary
Raurell-Torreda Marta, PhD
mraurell@ub.edu
626154955
Time Frame
Start Date: 2024-11-11
Estimated Completion Date: 2026-06-07
Participants
Target number of participants: 216
Treatments
Experimental: CBSD-experimental group
blood collection with Closed-Blood Sampling System (CBSD)
Active_comparator: Waste discard volume, control group
Blood collection without CBSD, usual practice, need to waste discard volume
Related Therapeutic Areas
Sponsors
Collaborators: Hospital General Universitario Gregorio Marañon, Hospital Universitario 12 de Octubre, Hospital Universitario Virgen Macarena, Hospital Universitario Rey Juan Carlos
Leads: University of Barcelona

This content was sourced from clinicaltrials.gov