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Clinical Trials/NCT06667310
NCT06667310
Completed
Not Applicable

Evaluatıon Of The Effect Of Neutrophıl/Lymphocyte, Platelet/Lymphocyte, Crp/Albumın, Base Defıcıt And Lactate Levels On Mortalıty Durıng The Admıssıon Of Trauma Patıents To Intensıve Care

Harran University1 site in 1 country150 target enrollmentNovember 5, 2024
ConditionsIntensive Care

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intensive Care
Sponsor
Harran University
Enrollment
150
Locations
1
Primary Endpoint
Primary outcome
Status
Completed
Last Updated
11 months ago

Overview

Brief Summary

Intensive care units are medical units where patients are closely monitored 24 hours a day due to critical health problems that threaten their lives and where rapid interventions are made when necessary. The clinical conditions of patients in these units can change rapidly. There are many studies in the literature indicating that inflammation indicators such as Neutrophil/Lymphocyte, Platelet/Lymphocyte and C-Reactive Protein/Albumin ratios and blood gas values such as Lactate and Base Deficit are simple, cheap and rapid biomarkers that can provide an early idea about the clinical course of patients.

Detailed Description

Intensive care units are medical units where patients are closely monitored 24 hours a day due to critical health problems that threaten their lives and where rapid interventions are made when necessary. The clinical conditions of patients in these units can change rapidly. There are many studies in the literature indicating that inflammation indicators such as Neutrophil/Lymphocyte, Platelet/Lymphocyte and C-Reactive Protein/Albumin ratios and blood gas values such as Lactate and Base Deficit are simple, cheap and rapid biomarkers that can provide an early idea about the clinical course of patients. The researchers aimed to evaluate the relationship between Neutrophil/Lymphocyte, Platelet/Lymphocyte and C-Reactive Protein/Albumin ratios and biomarkers such as Lactate and Base Deficit with the clinical course and survival of trauma patients admitted to the ICU and to see the compatibility of our data with the existing literature.

Registry
clinicaltrials.gov
Start Date
November 5, 2024
End Date
May 15, 2025
Last Updated
11 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Veli Fahri Pehlivan

Assistant Professor

Harran University

Eligibility Criteria

Inclusion Criteria

  • All trauma patients admitted to our general intensive care unit

Exclusion Criteria

  • Patients whose follow-up and treatment started and completed in the services.
  • Patients whose data is missing or whose data cannot be accessed.

Outcomes

Primary Outcomes

Primary outcome

Time Frame: one day

1. LACTATE LEVELS RATİO MEASUREMENT

Secondary Outcomes

  • seconary outcome(one day)

Study Sites (1)

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