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Clinical characteristics and prognosis of cancer patients with novel coronavirus pneumonia (COVID-19)

Screening and Identification of SARS-CoV-2 Infection and Progression in Cancer Patients Based on Bioinformatics Analysis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000030807
Enrollment
Unknown
Registered
2020-03-15
Start date
2020-02-15
Completion date
Unknown
Last updated
2020-03-16

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

non-cancer COVID-19 versus cancer with COVID-19:none

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
23 Years to 94 Years

Inclusion criteria

Inclusion criteria: 1. tumor group: (1) Aged >=18 years; (2) Diagnosed as a malignant tumor or has a history of malignant tumors before enrollment; (3) The diagnosis and treatment of new coronavirus pneumonia was issued in the seventh edition of the New Coronary Virus Pneumonia Diagnosis and Treatment Plan (trial implementation of the seventh edition) issued by the seventh edition of the National Health Committee in March 2020; (4) Life expectancy is at least 2 years. 2. Control group (non-tumor group): (1) Aged >=18 years; (2) no history of malignant tumors; (3) No basic diseases such as diabetes, coronary heart disease, pneumonia, chronic bronchitis; (4) The diagnosis and treatment of new coronavirus pneumonia was issued by the Seventh Edition of the National Health Committee of the People's Republic of China in March 2020 in the "Diagnosis and Treatment of New Coronavirus Pneumonia (Trial Version 7)"; (5) Life expectancy is at least 2 years.

Exclusion criteria

Exclusion criteria: (1) Those who do not meet the inclusion criteria of this study; (2) Complicated with severe primary heart, liver, and kidney disease; (3) Patients during perioperative period (within 7 days after operation); (4) Immune dysfunction diseases (such as systemic lupus erythematosus) in the active phase; (5) Those who lack clinical data or cannot obtain accurate data.

Design outcomes

Primary

MeasureTime frame
lynphocyte;cytokine;cancer history;order of severity;

Countries

China

Contacts

Public ContactZhihua Wang, Xianglin Yuan

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology(HUST)

zhwang_hust@hotmail.com+86 13607195518

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026