- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04383483
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
- Name: Ali Asan, MD
- Phone Number: +905332401067
- Email: draasan@yahoo.com
Study Contact Backup
- Name: Erkan Sayan, MD
- Phone Number: +905325972556
- Email: erkansayan@hotmail.com
Study Locations
-
-
Yildirim
-
Bursa, Yildirim, Turkey, 16350
- Recruiting
- Bursa Yuksek Ihtisas Training and Research Hospital
-
Contact:
- Ali Asan, MD
- Phone Number: +905332401067
- Email: draasan@yahoo.com
-
Contact:
- Halil Erkan Sayan, MD
- Phone Number: +905325972556
- Email: erkansayan@hotmail.com
-
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BYIEAH-202005
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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