COVID-19
Conditions
Brief summary
The goal of this observational study is to learn the long-term prognosis of patients and the clinical characteristics of complications, which is of great significance for treatment of novel coronavirus infection pneumonia. This trial plans to include 5700 inpatients with positive SARS CoV-2 nucleic acid test results. This trial does not involve the use of specific drug. Participants's health and psychological status will be observed at the preset time points. The blood, feces, urine samples of patients will be collected for relevant tests.
Detailed description
After the patients are enrolled, record the patient's treatment regimens, blood routine results, blood biochemistry results, cytokines results, lung imaging results, and cranial imaging results, understand the patient's current clinical manifestations, evaluate the patient's psychological status and quality of life, and collect samples of the patients' blood, feces, urine, and other related tests. Collection of clinical samples: collect blood, urine, throat swabs and other samples from patients with confirmed novel coronavirus pneumonia (Nucleic acid test positive), and collect samples for relevant tests at 3 months, 6 months, 12 months, 18 months, 24 months and 36 months after discharge of patients, and record the clinical manifestations of patients.
Interventions
None listed
Sponsors
Tongji Hospital
Study design
Observational model
OTHER
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients with confirmed COVID-19
Exclusion criteria
* Combined infection with influenza virus, mycoplasma, and chlamydia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| clinical manifestation | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
Secondary
| Measure | Time frame |
|---|---|
| cytokines level | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| psychological status | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| quality of life scores | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| cranial imaging results | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| lung imaging results | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| routine blood test results | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| treatment regimens | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| survival rate | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
| blood biochemistry results | 3 months, 6 months, 12 months, 18 months, 24 months, 36 months after patients discharge |
Countries
China
Contacts
Primary ContactQin Ning, Professor
Outcome results
None listed