Clinical Trials in Egypt / NCT07089524
Recruiting
Observational
A Comparative Study Between Neutrophil/Lymphocyte Ratio and Lactate/Albumin Ratio as Predictive Inflammatory Markers for Sepsis
NCT07089524 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
Sepsis
Study summary
Aim of this study is to predict the prognostic values of Neutrophil/ Lymphocyte ratio and Lactate/Albumin ratio in the outcome of patients with sepsis and septic shock with lower respiratory tract infection, also to compare between them regarding sensitivity and specificity.
Eligibility
Inclusion Criteria:
* Adults with lower respiratory tract infection
* Confirmed septic patients (under the third international consensus definitions of sepsis and septic shock),
* Admitted to intensive care unit.
* Age (18-80) years.
* Both genders.
Exclusion Criteria:
* Age: \< 18 years old, \> 80 years old
* Patient refusal.
* Pregnancy.
* Malignancy.
* Pathology that could affect serum albumin concentrations prior to ICU admission as Malnutrition
* Nephrotic syndrome
* Liver Cirrhosis
* Intestinal resection surgeries
Primary outcome measure(s)
- Detect the mortality due to sepsis with lower respiratory tract infection — From date of randomization until the date of death during the study period ( 12-18 months)
Detect the mortality due to sepsis and septic shock in patients with lower respiratory tract infection in ICU - The prognostic values of Neutrophil/Lymphocyte ratio and Lactate/Albumin ratio in Sepsis — From date of randomization until the date of discharge from the ICU or death during the study period ( 12-18 months )
predict the prognostic values of Neutrophil/Lymphocyte ratio and Lactate/Albumin ratio in the outcome of septic patients with lower respiratory tract infection in ICU
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Ain Shams university | Cairo | Abbassia | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07089524 on ClinicalTrials.gov ↗ ← All trials in Egypt