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OpenTrials
Terminated

NCT Number: NCT02417168

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

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.

Why the study stopped: PI left study site
Terminated

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Key information

Age range

Up to 17 year

Sex eligibility

All sexes

Study type

Observational

Primary location

CAMC Health Systems

Charleston, West Virginia, 25304, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children between the ages of birth to seventeen years.
  • Present to Charleston Area Medical Center Women and Children's Hospital
  • Existing pediatric oncology diagnosis.
  • Temperature greater than 38.0 C or 100.5 Fahrenheit.
  • Central venous access or functional port available.

Exclusion criteria

  • Any non-pediatric (eighteen years and above) oncology patient or a non-oncology patient.
  • The patient does not have central venous access or a port from which the blood can be drawn.

Treatment and study plan

Primary outcomes

  1. Change in procalcitonin levels

    Time frame: 24 hours

    Procalcitonin will be measured at the time of admission (Zero hours) and at 12, at 24 hours from admission.

Secondary outcomes

  1. The presence of bacteremia

    Time frame: 1 week

    Blood will be cultured for bacteria

Sponsors and collaborators

Lead sponsor

CAMC Health System

Other

Collaborators

  • CureSearch

Registry information

Official study title

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

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Apr 15, 2015
Registry last updated
Aug 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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