- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02352506
Serum MIF in Acute Kidney Injury
March 13, 2023 updated by: David M Baron, MD, PhD, Medical University of Vienna
Macrophage Migration Inhibitory Factor in the Serum of Critically Ill Patients as an Early Marker for Acute Kidney Injury
Acute kidney injury (AKI) is a common complication in critical care patients.
Currently no parameters are available for early prognosis of AKI.
Macrophage migration inhibitory factor (MIF) has been associated with AKI in clinical studies.
The aim of this study is to evaluate the time course of MIF concentrations in patients with AKI.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Vienna, Austria, 1090
- Medical University of Vienna
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Critical care patients
Description
Exclusion Criteria:
- Age < 18 years and > 80 years
- Patients with chronic dialysis
- Patients with continuous hemodialysis, hemofiltration or hemodiafiltration within 4 weeks prior to the study
- Patients with an expected length of ICU stay shorter than 3 days
- Patients with a low probability of surviving the first 2 days after ICU admission
- Pregnancy and nursing
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
AKI
Patients developing AKI during the ICU stay
|
Observational study, no intervention
|
|
No AKI
Matched controls not developing AKI during the ICU stay
|
Observational study, no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Macrophage migration inhibitory factor
Time Frame: Up to 14 days
|
Up to 14 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Serum creatinine
Time Frame: Up to 14 days
|
Up to 14 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2015
Primary Completion (Actual)
November 1, 2019
Study Completion (Actual)
January 1, 2023
Study Registration Dates
First Submitted
January 28, 2015
First Submitted That Met QC Criteria
January 28, 2015
First Posted (Estimate)
February 2, 2015
Study Record Updates
Last Update Posted (Actual)
March 15, 2023
Last Update Submitted That Met QC Criteria
March 13, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1680/2014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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