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OpenTrials
Completed

NCT Number: NCT04393974

COVID-19 and Cancer Patients

Routinely collected data will be used to assess the morbidity and mortality of cancer patients following a positive COVID-19 infection.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Institut Jules Bordet, Brussels, Belgium

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About this study

The SARS-CoV-2, (COVID-19) virus of the coronavirus family is believed to have been transmitted from animal to human. On 12th March 2020, the World Health Organisation (WHO) declared this particular coronavirus outbreak a pandemic.

How COVID-19 affects people is still not widely understood. Some people who have tested positive for the virus have been asymptomatic while others, who were otherwise well and healthy before infection, have died. Currently, information obtained so far suggests that most COVID-19 illness, however older people and people with severe comorbidities such as heart and lung disease and diabetes, seem to be at higher risk of developing serious COVID-19 illness.

This research is a retrospective, non-interventional study whose aim is to describe the features of COVID-19 infection specifically in cancer patients; to investigate its severity in this particular population and evaluate the long-term outcomes by means of medical charts review of consecutive patients co-diagnosed with SARS-CoV-2 infection and malignancy.

Patients will be identified from electronic medical records and entered into a pre-designed database. All information used will have been previously collected as part of routine standard of care and will involve but is not limited to: blood test results, prior and current anti-cancer therapy, medical history and most importantly clinical outcomes, such as response to any treatment provided for COVID-19 and patients' survival in relation to baseline clinic-pathologic profile. All data will be collected by each patient's team and will be anonymised and stored in a password-protected NHS computer.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

The investigators will evaluate and include consecutive patients observed in the outpatients and inpatients facility of the study centre meeting all the following CRITERIA:

  • Be ≥18 years of age.
  • Have a confirmed diagnosis of malignancy of any type.
  • Have a confirmed diagnosis of SARS-CoV-2 infection.

Exclusion criteria

Patients will not be entered in the study database when one or more of the following CRITERIA are present:

  • Unconfirmed diagnosis of SARS-CoV-2 infection
  • Insufficient clinical/follow up data.

Treatment and study plan

Primary outcomes

  1. Describe presenting characteristics and severity or SARS-CoV-2 infection in patients with cancer

    Time frame: 2 years

    Compiling a list of symptoms experienced by patients recruited onto the trial

  2. Assessing what factors are involved in prognosis of cancer patients with COVID-19

    Time frame: 2 years

    Evaluate prognostic factors for survival in patients with SARS-CoV-2 infection and cancer

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Registry information

Official study title

OnCovid: Natural History and Outcomes of Cancer Patients During the COVID19 Epidemic

Acronym: OnCovid

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
May 19, 2020
Registry last updated
Feb 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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