CClinicalTrials.gg
RecruitingNCT06082661Updated Dec 6, 2024

Blood Collection for COM/BSBS

An observational study in Healthy, sponsored by University of Central Florida. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-12-06.

Sponsored by University of Central Florida · Observational

From the registry’s dates

  • Started Jun 2022; still recruiting 4 years 3 months later.
Study type
Observational
Model
Other
Time perspective
Other
Enrollment
5,000
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Healthy

Keywords

  • Blood
  • Healthy
03

In context

Lead sponsor

University of Central Florida is the lead sponsor of 99 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

This study does not specifically target a particular vulnerable population.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • pregnant/suspect to be pregnant
  • prisoners
  • have donated blood anywhere in the preceding 16 weeks
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
5,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Acquisition of blood samples for testing

    This is a non-clinical, biospecimen collection study.

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
  • University of Central Florida
    Orlando, Florida 32816, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 6, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06082661
Lead sponsor
University of Central Florida
Responsible party
Sponsor
First posted
Oct 13, 2023
Start date
Jun 23, 2022
Primary completion
Jun 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
Dec 6, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion