COVID-19 Blood Sample Collection

  • STATUS
    Recruiting
Updated on 19 February 2024

Summary

Help in the fight against COVID-19!
The Indiana Biobank is looking for volunteers who have recovered from COVID-19 and are willing to donate a blood sample to be used in research to improve testing and develop treatments for COVID-19. 
 
The Indiana Biobank is a ‘bank’ of blood and other samples linked to health data. Approved researchers can access these samples and data to better understand this virus and resulting health complications.

Description

For those interested in participating, study staff will explain the study and answer any questions. If a person chooses to donate blood, they will review and sign a consent document, and then be scheduled to come to University Hospital on the IUPUI campus to provide a small blood sample (just under three tablespoons). This study is open to adults and children.
 
To participate, please complete the form below. If you have questions, please contact the Indiana Biobank directly via phone at 317-278-0880 or email at inbiobnk@iu.edu.  

FAQ


Details
Condition COVID,COVID-19,corona,coronavirus,corona virus,biobank,bio-specimen,biospecimen,COVID19,COVID 19
Age 18years - 100years
Clinical Study IdentifierTX11040
Last Modified on19 February 2024

Eligibility

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team


Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Preferred way of contact label
Please provide your preferred way of contact1234
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.