Effects of Neutrophil/Lymphocyte, Platelet/Lymphocyte, CRP/Albumin and Lactate on Mortality in Trauma Patients Admitted to Intensive Care
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
1 other identifier
observational
150
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 25, 2024
CompletedFirst Posted
Study publicly available on registry
October 31, 2024
CompletedStudy Start
First participant enrolled
November 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 10, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2025
CompletedMay 15, 2025
May 1, 2025
2 months
October 25, 2024
May 14, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Primary outcome
1\. LACTATE LEVELS RATİO MEASUREMENT
one day
Secondary Outcomes (1)
seconary outcome
one day
Eligibility Criteria
1-95 age intensive care patients
You may qualify if:
- \. All trauma patients admitted to our general intensive care unit
You may not qualify if:
- \- 1. Patients whose follow-up and treatment started and completed in the services.
- \. Patients whose data is missing or whose data cannot be accessed.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Veli Fahri Pehlivan
Karaköprü, Şanliurfa, 63100, Turkey (Türkiye)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
October 25, 2024
First Posted
October 31, 2024
Study Start
November 5, 2024
Primary Completion
January 10, 2025
Study Completion
May 15, 2025
Last Updated
May 15, 2025
Record last verified: 2025-05