MedTrace Logo

Transfusion Practices in Intensive Care Units: a Hungarian Nationwide Survey

NCT07532772 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 97

Last updated 2026-04-16

No results posted yet for this study

Summary

The aim of our data analysis-based questionnaire study is to assess the daily transfusion practices used in the care of critically ill patients in intensive care units in Hungary.

The rate and frequency of the application of physiological parameters (serum lactate level, central venous oxygen saturation and arteriovenous carbon dioxide difference, arteriovenous oxygen content difference) recommended as transfusion triggers in the international literature in daily practice will be assessed.

The aim of our survey is not only to collect statistical data, but also to map practical experiences, knowledge, opinions and possible institutional differences. Our aim is to obtain a more comprehensive picture of the operation of the care system, including transfusion activities, and any possible different practices applied in individual institutions, based on the experiences and observations of colleagues directly involved in patient care.

Conditions

  • Questionnaire and Survey
  • Central Venous Oxygen Saturation
  • Anaemia
  • Lactate
  • Transfusion

Interventions

OTHER

Survey using a questionnaire.

The questionnaire consists of 15 mandatory and 1 optional question.

Sponsors & Collaborators

  • Pest County Flór Ferenc Hospital

    lead OTHER

Principal Investigators

  • Zoltán Ruszkai, MD, PhD · Flór Ferenc Hospital Kistarcsa

  • Csanád Geréd, MD · Flór Ferenc Hospital Kistarcsa

Eligibility

Min Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-07-01
Primary Completion
2025-09-30
Completion
2025-09-30

Countries

  • Hungary

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07532772 on ClinicalTrials.gov