Blood collection from healthy adult volunteers
Blood Collection for Use with Translational, Biomedical Research At UCF College of Medicine and Burnett School of Biomedical Sciences
This study is collecting blood samples from healthy adults to help researchers at the University of Central Florida learn more about diseases and develop new ways to diagnose and treat them.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Central Florida Academic / other |
| Locations | 1 site (Orlando, Florida) |
| Trial ID | NCT06082661 on ClinicalTrials.gov |
What this trial studies
This observational study aims to collect blood samples from adult volunteers to support various biomedical and translational research projects at the University of Central Florida's College of Medicine and Burnett School of Biomedical Sciences. The collected biospecimens will be used for testing in separate IRB-approved protocols, focusing on understanding human diseases and developing innovative diagnostic and treatment methods. The research encompasses key areas such as cancer, cardiovascular health, immunity, neuroscience, and molecular microbiology.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy adults aged 18 years or older who weigh over 110 pounds and can provide informed consent.
Not a fit: Patients who are pregnant, prisoners, or have donated blood in the past 16 weeks may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of human diseases and lead to improved diagnostic and treatment methods.
How similar studies have performed: Other studies involving biospecimen collection for biomedical research have shown success in advancing medical knowledge and treatment options.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Orlando, Florida
- University of Central Florida — Orlando, Florida, United States (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.