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The Effect of COVID-19 Patients' Serum Phosphate Level on Mortality in ICU

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04800770
Recruitment Status : Recruiting
First Posted : March 16, 2021
Last Update Posted : March 16, 2021
Sponsor:
Information provided by (Responsible Party):
ismail aytaç, Ankara City Hospital Bilkent

Brief Summary:
The investigators aimed to investigate the relationship between phosphate level and mortality using the 4C Mortality Score in COVID-19 patients who were followed up in the intensive care unit.

Condition or disease Intervention/treatment
Phosphate Deficiency Covid19 Mortality Diagnostic Test: 4C mortality score

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Study Type : Observational [Patient Registry]
Estimated Enrollment : 160 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Target Follow-Up Duration: 6 Months
Official Title: Phosphate Levels of COVID-19 Patients and Mortality
Actual Study Start Date : March 3, 2021
Estimated Primary Completion Date : June 15, 2021
Estimated Study Completion Date : July 31, 2021

Resource links provided by the National Library of Medicine



Intervention Details:
  • Diagnostic Test: 4C mortality score
    4C mortality score and phosphate levels


Primary Outcome Measures :
  1. 4C mortality score [ Time Frame: 6 months ]
    4C Mortality Scores of the patients will be calculated, according to age, gender, number of comorbidities, respiratory rate, SpO2, GCS, urea, and CRP parameters

  2. serum phosphate levels [ Time Frame: 6 months ]
    mg/dl

  3. mortality [ Time Frame: 28 days ]
    mortality percentage of patients in 28 days



Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Participants hospitalized in the intensive care unit diagnosed with COVID-19 will incluse in the study
Criteria

Inclusion Criteria:

  • Participants hospitalized in the intensive care unit diagnosed with COVID-19 will incluse in the study

Exclusion Criteria:

  • there is no exclusion criteria

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04800770


Contacts
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Contact: betül aytaç, MD +905073578351 drbguven@hotmail.com
Contact: ismail aytaç, MD +905056340369 aytacismail1972@gmail.com

Locations
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Turkey
Ankara City Hospital Recruiting
Ankara, Turkey, 06800
Contact: İsmail Aytac    +905056340369    aytacismail1972@gmail.com   
Sponsors and Collaborators
Ankara City Hospital Bilkent
Investigators
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Principal Investigator: betül aytaç, MD ankara ch bilkent
Publications of Results:
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Responsible Party: ismail aytaç, medical doctor, Ankara City Hospital Bilkent
ClinicalTrials.gov Identifier: NCT04800770    
Other Study ID Numbers: E1-21-1584
First Posted: March 16, 2021    Key Record Dates
Last Update Posted: March 16, 2021
Last Verified: March 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by ismail aytaç, Ankara City Hospital Bilkent:
COVID19
phosphate deficiency
4C mortality score
Additional relevant MeSH terms:
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COVID-19
Respiratory Tract Infections
Infections
Pneumonia, Viral
Pneumonia
Virus Diseases
Coronavirus Infections
Coronaviridae Infections
Nidovirales Infections
RNA Virus Infections
Lung Diseases
Respiratory Tract Diseases