Clinical Trials Directory

Trials / Terminated

TerminatedNCT02417168

Procalcitonin Levels as a Predictor of Bacteremia in Febrile Pediatric Oncology Patients-Pilot Study

Procalcitonin Levels as a Predictor of Bacteremia in Febrile Pediatric Oncology Patients - Pilot Study

Status
Terminated
Phase
Study type
Observational
Enrollment
1 (actual)
Sponsor
CAMC Health System · Academic / Other
Sex
All
Age
17 Years
Healthy volunteers
Not accepted

Summary

Fevers raise the concern for serious bacterial infections in pediatric oncology patients receiving chemotherapy. The gold standard for diagnosing bacteremia (bacterial infection of the blood) is a blood culture. However, bacterial growth may not occur for 48 hours or there can be a false negative result. Thus, the biomarker, procalcitonin, has been investigated for its predictive ability to identify bacteremia earlier than blood culture. We believe that procalcitonin can assist in differentiating bacteremia from non-bacteremia infections in febrile pediatric oncology patients. A reliable predictor of bacteremia infections in pediatric oncology patients should decrease hospitalizations for fever and unnecessary antibiotic treatment. In our study we will measure procalcitonin levels in pediatric oncology patients presenting with fever. We will measure procalcitonin at the time of admission which is part of our standard of care for febrile pediatric oncology admissions. For the purpose of our study, we will additionally measure procalcitonin levels at 12 hours and at 24 hours post admission. We will examine procalcitonin levels at these three timepoints to determine if elevated procalcitonin levels predict bacteremia in pediatric oncology patients with and without neutropenia.

Conditions

Timeline

Start date
2015-07-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2015-04-15
Last updated
2020-03-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02417168. Inclusion in this directory is not an endorsement.