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COVID-19 in Cancer Patients: Evaluation of Clinical Course and Impact on Oncological Care Including Biobanking (COVIDHELP)

U

Universitätsklinikum Hamburg-Eppendorf

Status

Unknown

Conditions

COVID
Cancer

Treatments

Other: No Intervention

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The COVIDHELP study will prospectively evaluate the yet unknown clinical course of the COVID-19 infection in cancer patients and document the impact of potential infrastructural limitations on cancer care of COVID-19 positive patients. All patients consenting will provide peripheral blood samples for prospective biobanking with the aim of investigating immune response and immunity against COVID-19.

Full description

Based on patients, who are treated in the University Cancer Center Hamburg (UCCH) and its contracted partner network, which comprises all cancer treating departments at the University Medical Center of Hamburg-Eppendorf (UKE), as well as 19 office-based oncologists and 20 surrounding hospitals, recruitment for the study will be done as follows:

(i) as a cancer patient during regular aftercare appointments who reports a current or past COVID-19 infection.

(ii) as an acute COVID-19 patient who reports a prevalent cancer diagnosis

Data will be collected as available from routine clinical care and includes demographic and biometric data, medical history, baseline data at inclusion as well as inpatient and intensive care unit admissions. Upon consent, patients will provide peripheral blood samples at time of inclusion and after 6 month. Recruitment is limited to a one-year period (April 2020 - April 2021).

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key inclusion criteria:

  • Known diagnosis of cancer
  • Known diagnosis of CoVID-19 infection
  • Age ≥ 18 years
  • Signed informed consent

Key exclusion criteria:

• refusal of participation

Trial contacts and locations

1

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Central trial contact

Katja Weisel, MD; Niklas Boerschel, MD

Data sourced from clinicaltrials.gov

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