Actively Recruiting
Burden, Mortality and Supply Costs in Intensive Care Unit Patients. Health Services Research.
Led by University of Ulm · Updated on 2024-01-17
700
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to observe the relationship between different therapy strategies and treatment outcomes for patients in intensive care units (ICUs) under real-world conditions. It focuses on three initial risk groups—high, intermediate, and low—based on factors such as frailty, disease severity, and the number of organ systems requiring support. The study evaluates three key endpoints: burden of care, mortality, and supply costs. The study includes ICU patients who either stay for at least 72 hours or die within 72 hours of admission. Participants are categorized into risk groups according to the Clinical Frailty Scale, the Simplified Acute Physiology Score II, and the number of organ systems needing support or replacement. The study observes therapy strategies such as maximal therapy, withholding treatment, or withdrawing treatment, assessing their association with treatment success across these groups. Participants will be monitored over an 18-month period to measure burden of care, mortality rates, and supply costs. Data collection will occur under typical clinical conditions without altering standard care. The study systematically tracks patient outcomes related to therapy strategies, aiming to provide insights into intensive care practices and associated resource use.
CONDITIONS
Brief Title
Burden, Mortality and Supply Costs in Intensive Care Unit Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients dying on the ICU
- All patients staying for at least 72 hours on the ICU
You will not qualify if you...
- No
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 18 months
Participants who undergo routine intensive care are observed regarding their therapy strategies, risk groups, and outcomes over time.
Trial Site Locations
Total: 1 location
1
Department of Anaesthesiology, University Hospital Ulm
Ulm, Germany, 89075
Actively Recruiting
Research Team
M
Manfred Weiss, MD, MBA
E
Eberhard Barth, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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