Observational Cohort of COVID-19 Patients in Hubei Province
OCCP-HP
Observational Cohort of The Effects of Clinical Indicators, Drug Use and Genotypes on The Clinical Prognosis of COVID-19 Patients in Hubei Province
1 other identifier
observational
68,000
1 country
1
Brief Summary
This study intends to use the relevant case data of COVID-19 in Hubei Province, using big data processing and mining methods to evaluate the effects of clinical indicators, drug use and genes on the clinical prognosis of COVID-19 patients, so as to provide a theoretical basis for the treatment of these diseases and reduce the mortality.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2020
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2020
CompletedFirst Submitted
Initial submission to the registry
November 10, 2022
CompletedFirst Posted
Study publicly available on registry
November 14, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2024
CompletedMarch 7, 2024
March 1, 2024
4.1 years
November 10, 2022
March 6, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
All-cause mortality
Numbers and dates of death in each group
2 years
Study Arms (1)
patients with coronavirus disease 2019 (COVID-19)
Patients diagnosed with COVID-19 in Hubei Province
Interventions
Eligibility Criteria
This study is a hospital-based observational study initiated by Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology. Trained researchers are responsible for screening and joining the group. About 6,8000 COVID-19 patients in Hubei Province were expected to be included in this study. Patients enrolled in the group will undergo baseline survey and follow-up according to the program.
You may qualify if:
- Age ≥ 18, regardless of gender;
- A history of epidemiology, including travel or residence in high-risk areas or other communities with case reports within 14 days before the onset of the disease, or have a history of contact with novel coronavirus infection (those who are positive for nucleic acid tests); or patients with fever or respiratory symptoms from the community with case reports; or aggregative onset;
- Corresponding clinical manifestations, including respiratory symptoms such as fever, with typical imaging features of COVID-19, normal or decreased white blood cell count and decreased lymphocyte count in the early stage of the disease;
- Clear etiological evidence, including real-time fluorescent RT-PCR detection of novel coronavirus nucleic acid positive, or viral gene sequencing, is highly homologous to novel coronavirus.
You may not qualify if:
- Patients who meet any of the following criteria cannot be enrolled in this study:
- Patients refused to participate in this study;
- According to the researchers, patients are unable to complete this study or comply with the requirements of this study (due to management or other reasons).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dao Wen Wanglead
Study Sites (1)
Tongji Hospital
Wuhan, Hubei, 430030, China
Related Publications (2)
Li D, He W, Yu B, Wang DW, Ni L. NT-proBNP ratio is a potential predictor for COVID-19 outcomes in adult Chinese patients: a retrospective study. Sci Rep. 2024 Mar 11;14(1):5906. doi: 10.1038/s41598-024-56329-2.
PMID: 38467760DERIVEDXu K, He W, Yu B, Zhong K, Zhou D, Wang DW. Beneficial Effects of Angiotensin II Receptor Blockers on Mortality in Patients with COVID-19: A Retrospective Study from 2019 to 2020 in China. Cardiovasc Drugs Ther. 2025 Feb;39(1):63-74. doi: 10.1007/s10557-023-07494-5. Epub 2023 Aug 11.
PMID: 37566218DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Prof.
Study Record Dates
First Submitted
November 10, 2022
First Posted
November 14, 2022
Study Start
February 1, 2020
Primary Completion
March 1, 2024
Study Completion
March 1, 2024
Last Updated
March 7, 2024
Record last verified: 2024-03