Procalcitonin as a Prognostic Predictor in Patients With Acute Infectious Disease Hospitalized in the Internal Medicine Department.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBarzilai Medical Center

About this trial

Procalcitonin is a well-known biomarker used to distinguish between bacterial and viral infections, assess a patient's risk category, and serve as a prognostic indicator. However, existing data are derived primarily from relatively young patients in intensive care units; there is a lack of information regarding the prognostic significance of procalcitonin in older patients hospitalized in internal medicine wards.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All patients hospitalized in internal medicine and geriatric wards with a diagnosis of acute infectious disease who underwent procalcitonin testing, starting in 2020.

Disqualifiers

Age under 18

Extensive burns

Major operation in the last 30 days

Major trauma in the last 30 days.

Trial population

All patients hospitalized in internal medicine and geriatric wards with a diagnosis of acute infectious disease who underwent procalcitonin testing, starting in 2020.

Trial design

Design model

Case-only

Time perspective

Retrospective

Treatments tested in this trial

  • No Interventions

    Other intervention

    No intervention, retrospective observational study

Treatment groups

1,000 Participants
are divided into 1 treatment group
Group A: Positive Procalcitonin1 intervention

Trial outcomes

Primary outcomes

1

Mortality

Evaluation of procalcitonin as a prognostic marker in patients hospitalized in the internal medicine and geriatric department by examining mortality during hospitalization, within 7 days and within 30 months.

Time frame
30 days

Secondary outcomes

1

Additional Outcomes - Length of stay

Comparison of procalcitonin and CRP as predictors of length of hospital stay

Time frame
30 days
2

Additional data - morbidity

need for vasopressors or mechanical ventilation, need for intensive care, need for invasive intervention

Time frame
30 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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