CoV-ICU Score, Intensive Care Unit, SARS-CoV-2

March 26, 2021 updated by: Ali ASAN, Bursa Yüksek İhtisas Education and Research Hospital

CoV-ICU Score: Who Will Need Intensive Care in the Course of Corona Virus Disease?

In the course of COVID disease, some patients need intensive care treatment. We aim to find an answer to the question of whether the patient's CRP, ferritin, D-dimer, Oxygen Saturation, lymphocyte count, and body mass index can be used as a criterion for admitting patients with COVID to the intensive see unit.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

It is aimed to determine the patients who are above the threshold value to be determined according to this scoring result. Identifying patients who may need intensive care and following them closely will positively affect patient prognosis.

Study Type

Observational

Enrollment (Anticipated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Yildirim
      • Bursa, Yildirim, Turkey, 16350
        • Recruiting
        • Bursa Yuksek Ihtisas Training and Research Hospital
        • Contact:
        • Contact:
        • Principal Investigator:
          • Nermin Kelebek Girgin, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 100 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All patients admitted to the intensive care unit with the diagnosis of COVID

Description

Inclusion Criteria:

Patients admitted to the intensive care unit with the diagnosis of COVID

Exclusion Criteria:

<18 years patients

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
CoVID patients admitted to ICU
Patients admitted to the intensive care unit with the diagnosis of COVID
COVICU

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
COVICU score
Time Frame: 1 week
With this scoring, identifying patients who may need intensive care early and following them closely will have a positive effect on patient prognosis.
1 week
Values
Time Frame: 1 week
Minimum and maximum values will be determined at the end of the study. Higher scores mean a worse outcome
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ali Asan, MD, Bursa Yuksek Ihtisas Training and Research Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 15, 2020

Primary Completion (Anticipated)

January 31, 2022

Study Completion (Anticipated)

February 28, 2022

Study Registration Dates

First Submitted

May 7, 2020

First Submitted That Met QC Criteria

May 7, 2020

First Posted (Actual)

May 12, 2020

Study Record Updates

Last Update Posted (Actual)

March 29, 2021

Last Update Submitted That Met QC Criteria

March 26, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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