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A Study on the Prospective Cohort Library of COVID-19 in Southeran

A Study on the Prospective Cohort Library of Novel Coronavirus Pneumonia in Southeran

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04342702
Enrollment
504
Registered
2020-04-13
Start date
2020-03-16
Completion date
2021-03-31
Last updated
2020-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19, Follow-up, Infectious Diseases, Respiratory

Brief summary

This is a multi-centre population-based follow-up study for all 504 patients with laboratory-confirmed COVID-19. This study establishes a standardized and structured clinical database to provide complete and multidimensional clinical diagnosis and treatment data of novel coronavirus pneumonia, which also support future epidemiological, infectious disease study and patients' prognosis, by collecting clinical data and the related data of patients with novel coronavirus pneumonia in Southern Zhejiang province.

Detailed description

The follow-up information will be collected in one-month, three-month, six-month and one-year after discharge. Information about symptoms, radiographic and laboratory findings, lung function, SF-36 QUESTIONNAIRE, antibody of COVID19,result of RT-PCR Test and suvival information will be collected through all time frames.

Interventions

None listed

Sponsors

Wenzhou Medical University
CollaboratorOTHER
First Affiliated Hospital of Wenzhou Medical University
CollaboratorOTHER
Wenzhou Central Hospital And Sixth People's Hospital of Wenzhou Medical University
CollaboratorUNKNOWN
Yueqing Hospital of Wenzhou Medical University
CollaboratorUNKNOWN
Ruian Hospital of Wenzhou Medical University
CollaboratorUNKNOWN
Cangnan Hospital of Wenzhou Medical University
CollaboratorUNKNOWN
Pingyang Hospital of Wenzhou Medical University
CollaboratorUNKNOWN
Yongjia People's Hospital
CollaboratorUNKNOWN
Second Affiliated Hospital of Wenzhou Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients with laboratory-confirmed COVID-19 in Wenzhou

Exclusion criteria

* Suspected cases of COVID-19

Design outcomes

Primary

MeasureTime frameDescription
36-Item Short Form Survey Instrument (SF-36)one month, three month, six month and one year after discharge, minimum scoresum score of SF 36 form in each time frame
the value of FEV1 by lung function testone month, three month, six month and one year after discharge
the ratio of FEV1 to FVC by lung function testone month, three month, six month and one year after discharge

Secondary

MeasureTime frameDescription
Neutrophil valueone month, three month, six month and one year after dischargelaboratory result
DDI valueone month, three month, six month and one year after dischargelaboratory result
the proportion of applying ACEIs/ARBs medicationfrom the date of hospital admission to the day of hospital dischargecollect the number of applying ACEIs/ARBs medication and calculate the proportion
the predicted value of FEV1 by lung function testone month, three month, six month and one year after discharge
number of cases returning to positive result in RT-PCR testone month, three month, six month and one year after discharge
Number of positive outcome of IgG for antibody of COVID-19one month, three month, six month and one year after discharge
number of clinical symptoms after hospital dischargeone month, three month, six month and one year after dischargeclinical symptoms
the predicted ratio of FEV1 to FVC by lung function testone month, three month, six month and one year after discharge
Lymphocyte valueone month, three month, six month and one year after dischargelaboratory result

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026