NCT06912204

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
85

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 15, 2025

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

March 29, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 4, 2025

Completed
Last Updated

June 15, 2025

Status Verified

June 1, 2025

Enrollment Period

4 months

First QC Date

March 29, 2025

Last Update Submit

June 12, 2025

Conditions

Keywords

mturtic scoreintensiva caremortality

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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)

Location

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

patient outcome data

Shared Documents
STUDY PROTOCOL

Locations