Serum Procalcitonin Level May Predict Acute Kidney Injury in ICU Patients With Sepsis
NCT ID: NCT03097393
Last Updated: 2017-03-31
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
67 participants
OBSERVATIONAL
2014-01-01
2017-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
AKI GROUP
measure Procalcitonin among Patient developed Acute kidney injury during ICU stay
measure Serum procalcitonin level
measuring procalcitonin level
Non-AKI group
measure Procalcitonin among Patient did not develop Acute kidney injury during ICU stay
measure Serum procalcitonin level
measuring procalcitonin level
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
measure Serum procalcitonin level
measuring procalcitonin level
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Patients on Renal replacement therapy
* patients without procalcitonin level within 24 hours from admission.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Benha University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mahmoud Hamada imam
Lecturer in Internal Medidicne Department- Faculty of Medicine
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Benha317
Identifier Type: -
Identifier Source: org_study_id