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

Sponsor
Universitätsklinikum Hamburg-Eppendorf (Other)
Overall Status
Unknown status
CT.gov ID
NCT04408339
Collaborator
University of Schleswig-Holstein, Campus Lübeck (Other), Universitätsklinikum Schleswig-Holstein, Campus Kiel (Other)
500
1
24
20.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: No Intervention

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).

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
COVID-19 Disease in Cancer Patients: Evaluation of Clinical Course and Impact on Oncological Care in the Hamburg Metropolitan Area Including Prospective Biobanking
Actual Study Start Date :
Apr 15, 2020
Anticipated Primary Completion Date :
Apr 14, 2021
Anticipated Study Completion Date :
Apr 14, 2022

Outcome Measures

Primary Outcome Measures

  1. Rate of hospitalization [2 years]

    Measured in percentage

  2. Duration of hospitalization [2 years]

    Measured in days from date of admission to definitive discharge

  3. Rate of admission to intensive care unit [2 years]

    Measured in percentage

  4. Length of stay in intensive care unit [2 years]

    Measured in days from date of admission to intensive care unit to the date of discharge

  5. Need of mechanical ventilation [2 years]

    Measured in percentage

  6. Duration of mechanical ventilation [2 years]

    Measured in days from the date of intubation to the stop date of mechanical ventilation

  7. Disease-specific mortality rate [2 years]

    COVID-19 associated mortality rate

Secondary Outcome Measures

  1. Rate of patients, whose oncologic treatment had to be modified due to COVID-19 [2 years]

    Measured in percentage. Modification is defined as cancellation, postponement or dose-adjustment of treatment.

  2. Cellular and humoral immune response to COVID-19 infection [6 month]

    Analysis of blood samples at time of diagnosis and after 6 month

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Hamburg Eppendorf Hamburg Germany

Sponsors and Collaborators

  • Universitätsklinikum Hamburg-Eppendorf
  • University of Schleswig-Holstein, Campus Lübeck
  • Universitätsklinikum Schleswig-Holstein, Campus Kiel

Investigators

  • Principal Investigator: Katja Weisel, MD, University Medical Center of Hamburg-Eppendorf

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Universitätsklinikum Hamburg-Eppendorf
ClinicalTrials.gov Identifier:
NCT04408339
Other Study ID Numbers:
  • PV7313
First Posted:
May 29, 2020
Last Update Posted:
Jun 16, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 16, 2020