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Clinical Trials/NCT06082661
NCT06082661
Recruiting
Not Applicable

Blood Collection for Use with Translational, Biomedical Research At UCF College of Medicine and Burnett School of Biomedical Sciences

University of Central Florida1 site in 1 country5,000 target enrollmentJune 23, 2022
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
University of Central Florida
Enrollment
5000
Locations
1
Primary Endpoint
Acquisition of blood samples for testing
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The objective of this biospecimen collection protocol is the acquisition of blood from adult volunteers. These biospecimens will be transferred to the College of Medicine (COM)/Burnett School of Biomedical Sciences (BSBS) research scientists and their research teams for testing according to their separate IRB-approved/exempted protocols. These separate IRBapproved protocols cannot be for genetic testing.

Detailed Description

Research scientists of the University of Central Florida College of Medicine (COM) and Burnett School of Biomedical Sciences (BSBS) conduct laboratory studies in biomedical and translational research for the purpose of understanding human disease and developing innovative methods for diagnosing, measuring, or treating disease or disease symptoms. The key research divisions are cancer, cardiovascular, immunity and pathogenesis, neuroscience, and molecular microbiology. Frequently, these studies require human blood (or its derivatives) for testing of assays and devices.

Registry
clinicaltrials.gov
Start Date
June 23, 2022
End Date
June 2027
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female adults
  • 18 years old or older
  • weigh over 110 pounds
  • able to provide informed consent

Exclusion Criteria

  • pregnant/suspect to be pregnant
  • prisoners
  • have donated blood anywhere in the preceding 16 weeks

Outcomes

Primary Outcomes

Acquisition of blood samples for testing

Time Frame: 5 years

This is a non-clinical, biospecimen collection study.

Study Sites (1)

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