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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04366024
Other study ID # XQonc-016
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 17, 2020
Est. completion date December 31, 2021

Study information

Verified date February 2024
Source Xinqiao Hospital of Chongqing
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Investigators use clinical data from a large sample of COVID-19 disease patients to screen out biomarkers associated with disease severity. Then, a novel nomogram model will be established to predict covid-19 disease severity, which could provide important assistance and supplement for clinical work. In the case of extremely shortage of front-line medical resources, patients with potential severe diseases will be timely treated with the help of the novel nomogram model.


Recruitment information / eligibility

Status Completed
Enrollment 1000
Est. completion date December 31, 2021
Est. primary completion date August 30, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - COVID-19 disease patients confirmed by virus nucleic acid RT-PCR and CT Exclusion Criteria: - unconfirmed suspected cases - Patients during pregnancy and lactation - incomplete clinical data - investigators considered patients ineligible for the trial - Child patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
other
clinical diagnosis

Locations

Country Name City State
China Xinqiao Hospital of Chongqing Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Xinqiao Hospital of Chongqing

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary the consistency of predicted severe rate and observed severe rate of COVID-19 patients We aim to use the clinical data of COVID-19 patients to construct a nomogram model to predict the severe rate of each patient, then the the consistency of predicted severe rate and observed severe rate will be evaluated by calibration plot. up to 3 months
Primary Duration of severe illness the duration of severe illness of each patient will evaluated up to 3 months
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