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Accurate Classification System for Patients With COVID-19 Pneumonitis

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. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04302688
Recruitment Status : Completed
First Posted : March 10, 2020
Last Update Posted : March 10, 2020
Sponsor:
Information provided by (Responsible Party):
Gong Qiong, Renmin Hospital of Wuhan University

Brief Summary:
The COVID-19 has a clustering morbidity trend and older people with chronic diseases are more likely to die, such as chronic renal insufficiency and chronic cardiovascular disease. We set up a COVID-19 pneumonia grading scale. The COVID-19 score system was validated to predict the clinical outcome of a patient.

Condition or disease
Pneumonitis

Detailed Description:
  1. First we collect the medical records, according to the time sequence, the patients were divided into two groups, one is the model group, and the other is the validate group.
  2. Responsible for the risk factor of regression equation according to the model. The patients were divided into three groups according to their total score of risk responsibility.
  3. Compared with SEPSIS and CURB-65 grading system with the grading system we established.

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Study Type : Observational
Actual Enrollment : 669 participants
Observational Model: Other
Time Perspective: Retrospective
Official Title: Accurate Classification System for Patients With COVID-19 Based on Prognostic Nomogram
Actual Study Start Date : December 10, 2019
Actual Primary Completion Date : February 10, 2020
Actual Study Completion Date : March 4, 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Pneumonia

Group/Cohort
modeling cohort
The 445 patients were grouped in chronological order.
validating colort
The remaining 224 patients.



Primary Outcome Measures :
  1. survival status [ Time Frame: 10 December 2019 to 10 February 2020 ]
    survival status as of February 24, 2020



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:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with novel coronavirus pneumonia, and all cases were collected from the People's Hospital of Wuhan University.
Criteria

Inclusion Criteria:

  • Patients with novel coronavirus pneumonia should be examined and diagnosed by CT and swab test of viral nucleic acid.

Exclusion Criteria:

  • Patients who should have died during the course of the disease, but the cause of death was unrelated to viral pneumonia.
  • Suspected patient review refers to the negative nucleic acid test.

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): NCT04302688


Locations
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China, Hubei
Renmin Hospital of Wuhan University
Wuhan, Hubei, China, 430060
Sponsors and Collaborators
Renmin Hospital of Wuhan University
Investigators
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Principal Investigator: Qiong Gong, MD. Renmin Hospital of Wuhan University
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Responsible Party: Gong Qiong, Professor, Renmin Hospital of Wuhan University
ClinicalTrials.gov Identifier: NCT04302688    
Other Study ID Numbers: COVID-19 WU1
First Posted: March 10, 2020    Key Record Dates
Last Update Posted: March 10, 2020
Last Verified: March 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: Not going to share for the time being.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Pneumonia
Lung Diseases
Respiratory Tract Diseases
Respiratory Tract Infections