Neutrophil Gelatinase Associated Lipocalin (NGAL) in Urine: Can This Prove to be a Biomarker for Acute Kidney Injury in Patients With Sepsis?
NCT ID: NCT02034240
Last Updated: 2015-04-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
21 participants
OBSERVATIONAL
2014-01-31
2015-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Neutrophile Gelatinase Associated Lipocalin Evaluation in Septic Acute Kidney Injury
NCT01122225
NGAL in Prediction of AKI and Patient Outcomes
NCT06691607
NGAL As An Aid for the Diagnosis of Acute Kidney Injury in Intensive Care
NCT02121470
Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Evolving Acute Kidney Injury
NCT00445809
Serum Neutrophil Gelatinase-associated Lipocalins (NGAL) and Chronic Kidney Disease
NCT04008810
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Septic shock
* Patients must not be able to give consent
Exclusion Criteria
* known kidney injury
* Fully alert patients that can give consent
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kolding Sygehus
OTHER
Sygehus Lillebaelt
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Claes Falkenberg Elvander
Medical Doctor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jannie Bisgaard Stæhr, PhD, M.D
Role: STUDY_CHAIR
Odense University Hospital
Claes Falkenberg Elvander, M.D
Role: STUDY_DIRECTOR
Kolding Sygehus
Srishamanthi Sriskandarajah, M.D
Role: PRINCIPAL_INVESTIGATOR
Kolding Sygehus
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faelles Akut Modtagelse, Kolding Sygehus
Kolding, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DNVK:1305 385
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.