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OpenTrials
Active, Not Recruiting

NCT Number: NCT04568148

COVID-19 Biorepository

Establish a COVID-19 biorepository to aid in developing our knowledge of the disease.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Kansas Medical Center

Kansas City, Kansas, 66160, United States

About this study

While SARS-CoV-2 has some similarities to the SARS-CoV pathogen that led to an epidemic in 2002 and 2003, there is much about the epidemiology, pathogenesis, clinical presentation, diagnosis, and treatment of the novel virus that remains unknown.3 Additional research is needed to explore the nature of the virus, its spectrum of disease, and potential therapies to combat its spread. The aim of this project will be to establish a biorepository of blood samples from patients infected with SARS-CoV-2 that can then be used by investigators to expand our understanding of COVID-19 and its treatment and, in turn, improve patient outcomes.

The COVID-19 biorepository will accomplish the following specific aims:

  • Establish a collection of biospecimens from patients with COVID-19.
  • Establish a link between biospecimens and longitudinal individual patient data, which will be collected and stored in RedCap.
  • Provide biospecimens and unique patient data to researchers investigating COVID-19. Separate IRB approval will be needed for these studies.

Who can participate

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

Inclusion criteria

  • The participant is a patient at TUKHS or has agreed to participate in a study approved by the KUMC Human Research Protection Program (HRPP).
  • The participant has a diagnosis of COVID-19 confirmed by COVID-19 PCR.
  • Patient is 18 years of age or older.

Exclusion criteria

  • Participant declines to participate (living patients only)
  • Participant or healthcare surrogate is unable to provide informed consent (living patients only)

Treatment and study plan

Primary outcomes

  1. Biospecimen Collection

    Time frame: From Enrollment to 3 Months

    Establish a collection of biospecimens from patients with COVID-19.

  2. Establishing Connections

    Time frame: From Enrollment to 3 Months

    Establish a link between biospecimens and longitudinal individual patient data

  3. Continuing COVID Research

    Time frame: From Enrollment to 3 Months

    Provide biospecimens and unique patient data to researchers investigating COVID-19

Sponsors and collaborators

Lead sponsor

University of Kansas Medical Center

Other

Registry information

Important dates

Study start
2020
Primary completion
2023
Study completion
2026
First posted
Sep 29, 2020
Registry last updated
May 22, 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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