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COVID19NCT04414657

USZ BioResource COVID-19

An observational study of COVID19, run by Regina Grossmann at 1 site in Switzerland.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

Mono-centric. Blood sampling for biobank development, including linkage to patient data (resource for research on COVID19). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
COVID19
What is being tested?
blood sampling for biobank
How many people
150 participants
Where
1 siteSwitzerland
Study dates
9 Apr 2020to 30 Sep 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: SARS-CoV-2 infektion (according to WHO guideline)

Who may be able to join

  • m/f age > 18 years
  • SARS-CoV-2 infektion (according to WHO guideline)
  • hospitalisation, general ward
  • acceptable language knowledge
  • voluntary IFC and biobank appendix

Who cannot join

  • contra indication for blood sampling

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • University Hospital Zurich, Clinical Trials Center

    Zurich, 8091

Other trials in Switzerland

About this study

Official title: Development of a SARS-CoV-2 Research Biobank and Databank

Mono-centric. Blood sampling for biobank development, including linkage to patient data (resource for research on COVID19).

Conditions
COVID19
Being tested
blood sampling for biobank
Medical subject headings
COVID-19

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • blood sampling for biobankOther

    blood sampling for biobank

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. blood sampling for biobank

    development of a biobank

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Jun 2020
  2. Study start9 Apr 2020
  3. Primary completion30 Sep 2021
  4. Study completion30 Sep 2021

Why it stopped: sufficient patient number reached; flattening out of pandemic in Switzerland

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
150 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04414657
Sponsor's protocol ID
CTC HFV2
Status last verified
Nov 2022
First submitted
2 Jun 2020
Last updated
14 Nov 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of COVID19, run by Regina Grossmann at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 14 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: sufficient patient number reached; flattening out of pandemic in Switzerland). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

blood sampling for biobank (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Nov 2022.

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