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Procalcitonin in patients with different types of severe infections

Not Applicable
Conditions
Health Condition 1: B998- Other infectious disease
Registration Number
CTRI/2023/05/052662
Lead Sponsor
BE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients aged >18 years

Patients with suspected infection presenting in ICU

Patients who got admitted to ICU for non-infectious cause and later acquiring nosocomial infections

Exclusion Criteria

Patients with the following findings will be excluded from the study

1. Who underwent major surgery in last 30 days prior to presentation 2. Severe trauma

3. Major burns

4. Non compliant dialysis dependent patients

5. Anaphylaxis

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Correlation of levels of Procalcitonin in patients suspected of having sepsis or septic shock caused by different species of pathogens including bacteria and fungi.Timepoint: At baseline
Secondary Outcome Measures
NameTimeMethod
To evaluate the association of PCT levels with severity of illness determined by SOFA score.Timepoint: 24 hours
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