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NCT06082661 Clinical Trial

Blood Collection for COM/BSBS

Healthy Clinical Trial

Official title:
Blood Collection for Use With Translational, Biomedical Research at UCF College of Medicine and Burnett School of Biomedical Sciences

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06082661
Other study ID # STUDY00003409
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 23, 2022
Est. completion date June 2027

Study information
Verified date October 2023
Source University of Central Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 5000
Est. completion date June 2027
Est. primary completion date June 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of Central Florida Orlando Florida

Sponsors (1)
Lead Sponsor Collaborator
University of Central Florida

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Acquisition of blood samples for testing This is a non-clinical, biospecimen collection study. 5 years
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