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

COVID-19 Disease in Cancer Patients: Evaluation of Clinical Course and Impact on Oncological Care in the Hamburg Metropolitan Area Including Prospective Biobanking

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04408339
Acronym
COVIDHELP
Enrollment
500
Registered
2020-05-29
Start date
2020-04-15
Completion date
2022-04-14
Last updated
2020-06-16

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

Conditions

Cancer, COVID

Brief summary

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.

Detailed 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).

Interventions

OTHERNo Intervention

No Intervention

Sponsors

University Hopsital Schleswig Holstein Campus Lübeck
CollaboratorOTHER
University Hospital Schleswig-Holstein
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Disease-specific mortality rate2 yearsCOVID-19 associated mortality rate
Need of mechanical ventilation2 yearsMeasured in percentage
Duration of mechanical ventilation2 yearsMeasured in days from the date of intubation to the stop date of mechanical ventilation
Rate of hospitalization2 yearsMeasured in percentage
Duration of hospitalization2 yearsMeasured in days from date of admission to definitive discharge
Rate of admission to intensive care unit2 yearsMeasured in percentage
Length of stay in intensive care unit2 yearsMeasured in days from date of admission to intensive care unit to the date of discharge

Secondary

MeasureTime frameDescription
Cellular and humoral immune response to COVID-19 infection6 monthAnalysis of blood samples at time of diagnosis and after 6 month
Rate of patients, whose oncologic treatment had to be modified due to COVID-192 yearsMeasured in percentage. Modification is defined as cancellation, postponement or dose-adjustment of treatment.

Countries

Germany

Contacts

Primary ContactKatja Weisel, MD
k.weisel@uke.de+49407410
Backup ContactNiklas Boerschel, MD
n.boerschel@uke.de+49407410

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026