NCT05719038

Brief Summary

The infection of COVID-19 has caused serious threat to the life and health of all mankind and increased huge economic burden. According to the current statistics, the incidence of pulmonary fibrosis after COVID-19 infection is about 27.7% -87%, 81% of severe patients and 37% of moderate patients have residual lung lesions, and 53% of patients still have residual lung abnormalities one year after infection, resulting in restrictive pulmonary dysfunction and affecting the health and life of patients. Therefore, it is very important to study the diagnostic and prognostic markers of pulmonary fibrosis after infection of COVID-19. At present, relevant studies have been carried out on imagomics and serum proteomics of pulmonary fibrosis after COVID-19 infection, and serum biomarkers and imagomics marker models for diagnosing pulmonary fibrosis after COVID-19 pneumonia have been developed. However, there are few studies combining imageomics and serum proteomics, and the mechanism of pulmonary fibrosis after COVID-19 has not been fully clarified. In this study, it is planned to recruit patients with moderate, severe and critical COVID-19 pneumonia infection, collect venous blood from subjects, and perform chest HRCT follow-up. Blood samples were screened by proteomics and verified by expanded samples to screen diagnostic and prognostic markers of pulmonary fibrosis after COVID-19 infection. At the same time, based on deep learning technology, a model was developed to predict the occurrence and prognosis of pulmonary fibrosis after infection of COVID-19 combined with clinical characteristics, serum markers and AI imagomics, so as to provide ideas for further elucidating the mechanism of occurrence and development of pulmonary fibrosis after infection of COVID-19.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2023

Geographic Reach
1 country

2 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 30, 2023

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

February 5, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 8, 2023

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2024

Completed
Last Updated

February 8, 2023

Status Verified

February 1, 2023

Enrollment Period

1.9 years

First QC Date

February 5, 2023

Last Update Submit

February 7, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • change of pulmonary fibrosis

    The change of pulmonary fibrosis were evaluated

    At the time of enrollment, The first month, the third month, the sixth month, the twelfth month

Secondary Outcomes (2)

  • change of protein in serum

    At the time of enrollment, the third month

  • changes of Lung function

    At the time of enrollment, the third month, the sixth month, the twelfth month

Study Arms (3)

Healthy control group

Diagnostic Test: observational study

Pulmonary fibrosis after COVID-19 Pneumonia

Diagnostic Test: observational study

No pulmonary fibrosis after COVID-19 Pneumonia

Diagnostic Test: observational study

Interventions

observational studyDIAGNOSTIC_TEST

observational study

Healthy control groupNo pulmonary fibrosis after COVID-19 PneumoniaPulmonary fibrosis after COVID-19 Pneumonia

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with newly diagnosed COVID-19 pneumonia were classified as moderate, severe and critical according to clinical classification, and underwent chest CT imaging follow-up and blood protein measurement. In the later stage, patients were divided into groups with pulmonary fibrosis and without pulmonary fibrosis according to whether pulmonary fibrosis occurred; Healthy people as healthy control groups.

You may qualify if:

  • age 18-90 years
  • novel coronavirus nucleic acid or antigen confirmed novel coronavirus infection
  • Meet the diagnostic criteria for moderate/severe/severe coronavirus infection in China (Trial Tenth Edition)
  • Chest CT showed that the extent of lung lesions was greater than 50%

You may not qualify if:

  • pregnant and lactating women
  • previous severe lung disease, such as known chronic lung disease: chronic obstructive pulmonary disease, asthma, interstitial lung disease, etc.
  • severe organ dysfunction: severe liver, kidney and heart dysfunction
  • severe epidemic defects (including tumors/severe rheumatism/organs, bone marrow transplantation/HIV, etc.)
  • inappropriate enrollment judged by the investigator

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

First Affiliated Hospital of Kunming Medical University

Kunming, Yunnan, 650000, China

Location

The First Affiliated Hospital of Kunming Medical University

Kunming, Yunnan, 650032, China

Location

Related Publications (5)

  • Xue M, Zhang T, Chen H, Zeng Y, Lin R, Zhen Y, Li N, Huang Z, Hu H, Zhou L, Wang H, Zhang XD, Sun B. Krebs Von den Lungen-6 as a predictive indicator for the risk of secondary pulmonary fibrosis and its reversibility in COVID-19 patients. Int J Biol Sci. 2021 Apr 10;17(6):1565-1573. doi: 10.7150/ijbs.58825. eCollection 2021.

  • Li X, Shen C, Wang L, Majumder S, Zhang D, Deen MJ, Li Y, Qing L, Zhang Y, Chen C, Zou R, Lan J, Huang L, Peng C, Zeng L, Liang Y, Cao M, Yang Y, Yang M, Tan G, Tang S, Liu L, Yuan J, Liu Y. Pulmonary fibrosis and its related factors in discharged patients with new corona virus pneumonia: a cohort study. Respir Res. 2021 Jul 9;22(1):203. doi: 10.1186/s12931-021-01798-6.

  • Yang J, Chen C, Chen W, Huang L, Fu Z, Ye K, Lv L, Nong Z, Zhou X, Lu W, Zhong M. Proteomics and metabonomics analyses of Covid-19 complications in patients with pulmonary fibrosis. Sci Rep. 2021 Jul 16;11(1):14601. doi: 10.1038/s41598-021-94256-8.

  • Sardar R, Sharma A, Gupta D. Machine Learning Assisted Prediction of Prognostic Biomarkers Associated With COVID-19, Using Clinical and Proteomics Data. Front Genet. 2021 May 20;12:636441. doi: 10.3389/fgene.2021.636441. eCollection 2021.

  • Bazdyrev E, Rusina P, Panova M, Novikov F, Grishagin I, Nebolsin V. Lung Fibrosis after COVID-19: Treatment Prospects. Pharmaceuticals (Basel). 2021 Aug 17;14(8):807. doi: 10.3390/ph14080807.

Related Links

MeSH Terms

Conditions

Pulmonary FibrosisCOVID-19

Condition Hierarchy (Ancestors)

Lung Diseases, InterstitialLung DiseasesRespiratory Tract DiseasesFibrosisPathologic ProcessesPathological Conditions, Signs and SymptomsPneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus Infections

Central Study Contacts

Jianqing Zhang, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 5, 2023

First Posted

February 8, 2023

Study Start

January 30, 2023

Primary Completion

December 30, 2024

Study Completion

December 30, 2024

Last Updated

February 8, 2023

Record last verified: 2023-02

Data Sharing

IPD Sharing
Will not share

Locations