Skip to content

The Diagnostic and Prognostic Utility of Procalcitonin (ProCT) for Ventilator-associated Pneumonia (VAP)

The Diagnostic and Prognostic Utility of Procalcitonin (ProCT) for Ventilator-associated Pneumonia (VAP)

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00498121
Enrollment
50
Registered
2007-07-09
Start date
2007-07-31
Completion date
2009-05-31
Last updated
2009-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventilator Associated Pneumonia

Keywords

Ventilator associated pneumonia., Procalcitonin.

Brief summary

Our aim in this study is to investigate the potential role of serum ProCT as an early diagnostic marker and later prognostic indicator for VAP.

Detailed description

Ventilator-associated pneumonia (VAP), a bacterial infection that develops after 48 hours or more of intubation, is associated with high morbidity and mortality. Rapid identification of VAP is required to improve survival and to reduce avoidable treatment-associated side effects. Procalcitonin (ProCT), a blood test, is a reasonably specific marker of bacterial infection and its level increases early in sepsis. In this study, a ProCT serum level will be measured in 50 patients with clinically suspected VAP. We aim to show that the ProCT level will be high early in VAP and will stay high in patients with poor prognosis. This will help to address the potential role of ProCT as part of early diagnosis and management of VAP.

Interventions

measuring PROCALCITONIN LEVEL

Sponsors

McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

In the preceding 24 h, the appearance of a new opacity or opacities on chest X-ray when compared to previous, and two of the following: 1. white blood cell count \> 12 or \< 5 x 10\^9 cells/L, 2. temperature \> 38°C or \< 35°C, or 3. purulent secretions.endotracheal samples must be collected by bronchoscope/bronchoalveolar lavage with quantitative culture or endotracheal aspiration with quantitative culture (when available) or qualitative culture from each patient to be enrolled in the study. This is a routine procedure done in every case of suspected VAP and is considered to be the standard of care.

Exclusion criteria

1. Known underlying chronic inflammatory condition of the lung (e.g., sarcoidosis, vasculitis) 2. Thyroid cancer patients 3. neutropenia (neutrophils \< 0.5 x 10\^9 cells/L 4. Concomitant AIDS 5. Solid organ transplantation with severe immunosuppression 6. New Antibiotic use for more than 18 hrs before blood sample collection 7. Severe pancreatitis 8. Attending physician does not agree with enrollment into the study.

Design outcomes

Primary

MeasureTime frame
Cases with VAP and high ProCT and Cases with Non-VAP and Low ProCTRetrospective chart review after results are available

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026