Actively Recruiting

All Genders
ID04094428

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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All patients dying on the ICU
  • All patients staying for at least 72 hours on the ICU
Not Eligible

You will not qualify if you...

  • No

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

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

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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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