Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:25 PM
Ignite Modification Date:
2025-12-24 @ 4:25 PM
NCT ID:
NCT02558166
Eligibility Criteria:
Inclusion Criteria:
First group (patients with shock):
* Critically ill patients admitted to the intensive care unit (ICU) with cardiogenic shock or shock due to sepsis/SIRS or hemorrhage
* Age \> 18 years
* Noradrenalin support
* ICU admission \< 24 hours
* Signed informed consent
Second group (patients without shock):
* Critically ill patients admitted to the intensive care unit (ICU) without shock, without vasopressor support and without fluid-dependent circulation
* Age \> 18 years
* ICU admission \< 24-h
* Signed informed consent
In both groups, written consent will be obtained if and when the patients are awake and able to communicate ('deferred consent')
Exclusion Criteria:
* Severe pre-admission chronic renal insufficiency (eGFR \< 30 ml/min)
* Dialysis dependency
* Renal transplantation
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02558166
Study Brief:
Protocol Section:
NCT02558166