Predictive Value of the mNutric Score and Survival Analysis in Critically Ill Patients Hospitalised in the Intensive Care Unit
1 other identifier
observational
85
1 country
1
Brief Summary
Our study is an observational study and the follow-up hematological tests of patients in the intensive care unit will be recorded during their first admission. In this study, routinely checked blood parameters in patients will be interpreted and mnutric scores created together with their clinical features will be recorded. Routine blood tests will be performed during these records and no intervention will be made. Only an observational study will be conducted.
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
Study Start
First participant enrolled
November 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 15, 2025
CompletedFirst Submitted
Initial submission to the registry
March 29, 2025
CompletedFirst Posted
Study publicly available on registry
April 4, 2025
CompletedJune 15, 2025
June 1, 2025
4 months
March 29, 2025
June 12, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
primer
It was aimed to investigate the mnutric scores of patients who survived and did not survive after 28 days of follow-up.
28-day follow-up period
Study Arms (2)
survived
non-survived
Patients who did not survive after 28 days
Eligibility Criteria
Critical care patients admitted to the intensive care unit and no deaths within 24 hours
You may qualify if:
- over 18 years old , Patients who have been hospitalized for more than 24 hours
You may not qualify if:
- under 18 years old, pregnancy patients, Patients hospitalized for less than 24 hours
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Amasya University Training and Research Hospital
Samsun, 55200, Turkey (Türkiye)
Related Publications (1)
Grillo-Ardila CF, Tibavizco-Palacios D, Triana LC, Rugeles SJ, Vallejo-Ortega MT, Calderon-Franco CH, Ramirez-Mosquera JJ. Early Enteral Nutrition (within 48 h) for Patients with Sepsis or Septic Shock: A Systematic Review and Meta-Analysis. Nutrients. 2024 May 22;16(11):1560. doi: 10.3390/nu16111560.
PMID: 38892494BACKGROUND
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 28 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- associate proffessor
Study Record Dates
First Submitted
March 29, 2025
First Posted
April 4, 2025
Study Start
November 1, 2024
Primary Completion
March 1, 2025
Study Completion
March 15, 2025
Last Updated
June 15, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
patient outcome data